A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv680003



Internal ID15069969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:189322786..189375191hg38UCSC Ensembl
Innerchr4:190243940..190296345hg19UCSC Ensembl
Innerchr4:190480934..190533339hg18UCSC Ensembl
Innerchr4:190619089..190671494hg17UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg3852406
hg1952406
hg1852406
hg1752406
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517295
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv680003
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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