A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3749614



Internal ID19047895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:164003651..164067748hg38UCSC Ensembl
Innerchr6:164424683..164488780hg19UCSC Ensembl
Innerchr6:164344673..164408770hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3864098
hg1964098
hg1864098
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1019703
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)nssv3749614
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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