A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700345



Internal ID15436997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:102483093..102488900hg38UCSC Ensembl
Innerchr13:103135443..103141250hg19UCSC Ensembl
Innerchr13:101933444..101939251hg18UCSC Ensembl
Innerchr13:101933444..101939251hg17UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg385808
hg195808
hg185808
hg175808
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524419
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700345
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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