A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702716



Internal ID15439368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:171483944..171573082hg38UCSC Ensembl
Innerchr4:172405095..172494233hg19UCSC Ensembl
Innerchr4:172641670..172730808hg18UCSC Ensembl
Innerchr4:172779825..172868963hg17UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg3889139
hg1989139
hg1889139
hg1789139
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526416
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702716
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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