A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701350



Internal ID15438002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75329934..75519068hg38UCSC Ensembl
Innerchr3:75379085..75568219hg19UCSC Ensembl
Innerchr3:75461775..75650909hg18UCSC Ensembl
Innerchr3:75461775..75650909hg17UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38189135
hg19189135
hg18189135
hg17189135
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517173
Supporting Variants
Samples
Known GenesFAM86DP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701350
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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