A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527602



Internal ID15454895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:80295117..80302905hg38UCSC Ensembl
Innerchr10:82054873..82062661hg19UCSC Ensembl
Innerchr10:82044853..82052641hg18UCSC Ensembl
Innerchr10:82044853..82052641hg17UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg387789
hg197789
hg187789
hg177789
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704064
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527602
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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