A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525521



Internal ID15452814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:60496527..60506388hg38UCSC Ensembl
Innerchr10:62256285..62266146hg19UCSC Ensembl
Innerchr10:61926291..61936152hg18UCSC Ensembl
Innerchr10:61926291..61936152hg17UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg389862
hg199862
hg189862
hg179862
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701654
Samples
Known GenesANK3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525521
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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