A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528006



Internal ID15455299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:9516262..9678218hg38UCSC Ensembl
Innerchr10:9558225..9720181hg19UCSC Ensembl
Innerchr10:9598231..9760187hg18UCSC Ensembl
Innerchr10:9598231..9760187hg17UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38161957
hg19161957
hg18161957
hg17161957
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704532
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528006
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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