A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696566



Internal ID15433218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:64043610..64058032hg38UCSC Ensembl
Innerchr10:65803370..65817792hg19UCSC Ensembl
Innerchr10:65473376..65487798hg18UCSC Ensembl
Innerchr10:65473376..65487798hg17UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3814423
hg1914423
hg1814423
hg1714423
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519093
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696566
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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