A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034064



Internal ID19123286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:66809380..66869989hg38UCSC Ensembl
Innerchr6:67519273..67579882hg19UCSC Ensembl
Innerchr6:67575994..67636603hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3860610
hg1960610
hg1860610
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3658757
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)nsv1034064
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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