A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704352



Internal ID15441004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:16028596..16087187hg38UCSC Ensembl
Innerchr21:17400916..17459507hg19UCSC Ensembl
Innerchr21:16322787..16381378hg18UCSC Ensembl
Innerchr21:16322787..16381378hg17UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3858592
hg1958592
hg1858592
hg1758592
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527854
Supporting Variants
Samples
Known GenesLINC00478
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704352
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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