A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv663971



Internal ID15053937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:8779046..8812681hg38UCSC Ensembl
Innerchr3:8820732..8854367hg19UCSC Ensembl
Innerchr3:8795732..8829367hg18UCSC Ensembl
Innerchr3:8795732..8829367hg17UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3833636
hg1933636
hg1833636
hg1733636
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517310
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv663971
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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