A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700695



Internal ID15437347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:32499498..32592485hg38UCSC Ensembl
Innerchr4:32501120..32594107hg19UCSC Ensembl
Innerchr4:32145018..32238005hg18UCSC Ensembl
Innerchr4:32291189..32384176hg17UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3892988
hg1992988
hg1892988
hg1792988
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524710
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700695
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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