A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3746763



Internal ID19045044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:149649..221515hg38UCSC Ensembl
Innerchr6:149649..221515hg19UCSC Ensembl
Innerchr6:94649..166515hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3871867
hg1971867
hg1871867
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1030207
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)nssv3746763
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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