A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697125



Internal ID15433777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:139175130..139178614hg38UCSC Ensembl
Innerchr4:140096284..140099768hg19UCSC Ensembl
Innerchr4:140315734..140319218hg18UCSC Ensembl
Innerchr4:140453889..140457373hg17UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg383485
hg193485
hg183485
hg173485
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519918
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697125
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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