A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694136



Internal ID15084102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:181478542..181500662hg38UCSC Ensembl
Innerchr4:182399695..182421815hg19UCSC Ensembl
Innerchr4:182636689..182658809hg18UCSC Ensembl
Innerchr4:182774844..182796964hg17UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg3822121
hg1922121
hg1822121
hg1722121
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522151
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694136
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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