A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030673



Internal ID19119892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:67835409..67932853hg38UCSC Ensembl
Innerchr6:68545302..68642745hg19UCSC Ensembl
Innerchr6:68602023..68699466hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3897445
hg1997444
hg1897444
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6013n100
Supporting Variantsnssv3747076, nssv3658794
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)nsv1030673
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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