A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017442



Internal ID19106659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:78148552..78318041hg38UCSC Ensembl
Innerchr6:78858269..79027758hg19UCSC Ensembl
Innerchr6:78914988..79084477hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38169490
hg19169490
hg18169490
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6024n100
Supporting Variantsnssv3659076
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)nsv1017442
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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