A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv437202



Internal ID15382508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:158520155..158520661hg38UCSC Ensembl
Outerchr1:158514588..158523364hg38UCSC Ensembl
Innerchr1:158489945..158490451hg19UCSC Ensembl
Outerchr1:158484378..158493154hg19UCSC Ensembl
Innerchr1:156756569..156757075hg18UCSC Ensembl
Outerchr1:156751002..156759778hg18UCSC Ensembl
Innerchr1:155706737..155707243hg16UCSC Ensembl
Outerchr1:155701170..155709946hg16UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg388777
hg198777
hg188777
hg168777
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv467083
SamplesNA10835
Known Genes
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)nsv437202
Frequency
Sample Size60
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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