A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv667155



Internal ID15057121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:137259590..137266198hg38UCSC Ensembl
Innerchr4:138180744..138187352hg19UCSC Ensembl
Innerchr4:138400194..138406802hg18UCSC Ensembl
Innerchr4:138538349..138544957hg17UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg386609
hg196609
hg186609
hg176609
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516176
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv667155
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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