A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018556



Internal ID19107773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:168829323..169023091hg38UCSC Ensembl
Innerchr6:169229418..169423186hg19UCSC Ensembl
Innerchr6:168971343..169165111hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38193769
hg19193769
hg18193769
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6202n100
Supporting Variantsnssv3653077
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)nsv1018556
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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