A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704347



Internal ID15440999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:17262929..17296010hg38UCSC Ensembl
Innerchr10:17304928..17338009hg19UCSC Ensembl
Innerchr10:17344934..17378015hg18UCSC Ensembl
Innerchr10:17344934..17378015hg17UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg3833082
hg1933082
hg1833082
hg1733082
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527849
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704347
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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