A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525597



Internal ID15452890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:100592028..100602358hg38UCSC Ensembl
Innerchr10:102351785..102362115hg19UCSC Ensembl
Innerchr10:102341775..102352105hg18UCSC Ensembl
Innerchr10:102341775..102352105hg17UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg3810331
hg1910331
hg1810331
hg1710331
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701740
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525597
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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