A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv679880



Internal ID15416532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:156652817..156652883hg38UCSC Ensembl
Innerchr4:157573969..157574035hg19UCSC Ensembl
Innerchr4:157793419..157793485hg18UCSC Ensembl
Innerchr4:157931574..157931640hg17UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3867
hg1967
hg1867
hg1767
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516423
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv679880
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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