A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3658817



Internal ID18957098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:74655473..74713171hg38UCSC Ensembl
Innerchr6:75365189..75422887hg19UCSC Ensembl
Innerchr6:75421909..75479607hg18UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3857699
hg1957699
hg1857699
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1015675
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)nssv3658817
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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