A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018836



Internal ID18761369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:121615257..121705135hg38UCSC Ensembl
Innerchr6:121936403..122026281hg19UCSC Ensembl
Innerchr6:121978102..122067980hg18UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3889879
hg1989879
hg1889879
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6142n100
Supporting Variantsnssv3654341
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)nsv1018836
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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