A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv437802



Internal ID15383108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:12610623..12610654hg38UCSC Ensembl
Outerchr16:12573219..12614437hg38UCSC Ensembl
Innerchr16:12704480..12704511hg19UCSC Ensembl
Outerchr16:12667076..12708294hg19UCSC Ensembl
Innerchr16:12611981..12612012hg18UCSC Ensembl
Outerchr16:12574577..12615795hg18UCSC Ensembl
Innerchr16:12670919..12670950hg16UCSC Ensembl
Outerchr16:12633515..12674733hg16UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg3841219
hg1941219
hg1841219
hg1641219
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv467683
SamplesNA19194
Known GenesSNX29
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)nsv437802
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