A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695967



Internal ID15432619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:155242752..155249207hg38UCSC Ensembl
Innerchr4:156163904..156170359hg19UCSC Ensembl
Innerchr4:156383354..156389809hg18UCSC Ensembl
Innerchr4:156521509..156527964hg17UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg386456
hg196456
hg186456
hg176456
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517632
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695967
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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