A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv437213



Internal ID15035945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:160692642..160705554hg38UCSC Ensembl
Outerchr1:160682940..160712046hg38UCSC Ensembl
Innerchr1:160662432..160675344hg19UCSC Ensembl
Outerchr1:160652730..160681836hg19UCSC Ensembl
Innerchr1:158929056..158941968hg18UCSC Ensembl
Outerchr1:158919354..158948460hg18UCSC Ensembl
Innerchr1:157879224..157892136hg16UCSC Ensembl
Outerchr1:157869522..157898628hg16UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3829107
hg1929107
hg1829107
hg1629107
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv467094
SamplesNA12707
Known GenesCD48
MethodSNP array
AnalysisOur algorithm aims to detect deletions that are transmitted from a hemizygous parent to a child. For each trio, every SNP was coded into one of seven categories: (A) Type I mendelian incompatibility (that is, consistent with deletion) involving mother; (B) Type I mendelian incompatibility involving father; (C) Type II mendelian incompatibility (that is, inconsistent with deletion); (D) child homozygous or missing data, both parents homozygous or missing data; (E) child homozygous or missing data, father heterozygous, mother homozygous or missing data; (F) child homozygous or missing data, mother heterozygous, father homozygous or missing data; (G) child heterozygous or both parents heterozygous (see Supplementary Methods for further details). SNPs were assigned to states D-G only if they did not contain mendelian incompatibilities. A run of consecutive SNPs in a particular trio was considered to be consistent with a maternal transmitted deletion if all SNPs were in states A, D or E, or with a paternal deletion if all SNPs were in states B, D or F.
PlatformNot reported
Comments
ReferenceConrad_et_al_2006
Pubmed ID16327808
Accession Number(s)nsv437213
Frequency
Sample Size60
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer