A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv655682



Internal ID15392334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:56569449..56713975hg38UCSC Ensembl
Innerchr10:58329209..58473735hg19UCSC Ensembl
Innerchr10:57999215..58143741hg18UCSC Ensembl
Innerchr10:57999215..58143741hg17UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38144527
hg19144527
hg18144527
hg17144527
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517747
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv655682
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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