A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026904



Internal ID19116122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:103271963..103314174hg38UCSC Ensembl
Innerchr6:103719838..103762049hg19UCSC Ensembl
Innerchr6:103826531..103868742hg18UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3842212
hg1942212
hg1842212
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6119n100
Supporting Variantsnssv3649894, nssv3649897, nssv3751266, nssv3649895, nssv3649893, nssv3751267, nssv3649896
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)nsv1026904
Frequency
Sample Size11257
Observed Gain6
Observed Loss1
Observed Complex0
Frequencyn/a


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