A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519864



Internal ID15447157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:97718324..97726887hg38UCSC Ensembl
Innerchr10:99478081..99486644hg19UCSC Ensembl
Innerchr10:99468071..99476634hg18UCSC Ensembl
Innerchr10:99468071..99476634hg17UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg388564
hg198564
hg188564
hg178564
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697091
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519864
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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