A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034012



Internal ID19123234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:137577090..137641116hg38UCSC Ensembl
Innerchr6:137898227..137962253hg19UCSC Ensembl
Innerchr6:137939920..138003946hg18UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg3864027
hg1964027
hg1864027
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6152n100
Supporting Variantsnssv3654414, nssv3654415
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)nsv1034012
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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