A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697116



Internal ID15433768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:71647461..71649687hg38UCSC Ensembl
Innerchr4:72513178..72515404hg19UCSC Ensembl
Innerchr4:72732042..72734268hg18UCSC Ensembl
Innerchr4:72878213..72880439hg17UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg382227
hg192227
hg182227
hg172227
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519903
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697116
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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