A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522710



Internal ID15450003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:3676972..3682419hg38UCSC Ensembl
Innerchr10:3719164..3724611hg19UCSC Ensembl
Innerchr10:3709164..3714611hg18UCSC Ensembl
Innerchr10:3709164..3714611hg17UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg385448
hg195448
hg185448
hg175448
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv706122
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522710
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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