A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3594606



Internal ID18892887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:62975756..63073436hg38UCSC Ensembl
Innerchr3:62961431..63059112hg19UCSC Ensembl
Innerchr3:62936471..63034152hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3897681
hg1997682
hg1897682
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1003613
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3594606
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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