A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv677967



Internal ID15414619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:42704111..42710097hg38UCSC Ensembl
Innerchr4:42706128..42712114hg19UCSC Ensembl
Innerchr4:42400885..42406871hg18UCSC Ensembl
Innerchr4:42547056..42553042hg17UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg385987
hg195987
hg185987
hg175987
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515863
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv677967
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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