A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3657579



Internal ID18955860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:61274104..61350771hg38UCSC Ensembl
Innerchr6:61886428..61963609hg19UCSC Ensembl
Innerchr6:61944387..62021568hg18UCSC Ensembl
Cytoband6q11.1
Allele length
AssemblyAllele length
hg3876668
hg1977182
hg1877182
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1022375
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)nssv3657579
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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