A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv668702



Internal ID15405354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:52036398..52037861hg38UCSC Ensembl
Innerchr20:50652937..50654400hg19UCSC Ensembl
Innerchr20:50086344..50087807hg18UCSC Ensembl
Innerchr20:50086344..50087807hg17UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg381464
hg191464
hg181464
hg171464
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515528
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv668702
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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