A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525005



Internal ID15452298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:93262833..93264169hg38UCSC Ensembl
Innerchr10:95022590..95023926hg19UCSC Ensembl
Innerchr10:95012580..95013916hg18UCSC Ensembl
Innerchr10:95012580..95013916hg17UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg381337
hg191337
hg181337
hg171337
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701040
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525005
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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