A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv656983



Internal ID15393635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:23651593..23722592hg38UCSC Ensembl
Innerchr4:23653216..23724215hg19UCSC Ensembl
Innerchr4:23262314..23333313hg18UCSC Ensembl
Innerchr4:23329485..23400484hg17UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3871000
hg1971000
hg1871000
hg1771000
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517733
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv656983
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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