A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700565



Internal ID15437217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:109543600..109617196hg38UCSC Ensembl
Innerchr10:111303358..111376954hg19UCSC Ensembl
Innerchr10:111293348..111366944hg18UCSC Ensembl
Innerchr10:111293348..111366944hg17UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg3873597
hg1973597
hg1873597
hg1773597
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524604
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700565
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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