A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016305



Internal ID19105524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:60691299..61119912hg38UCSC Ensembl
Innerchr6:57659046..58140430hg19UCSC Ensembl
Innerchr6:57767005..58248389hg18UCSC Ensembl
Cytoband6p11.2
Allele length
AssemblyAllele length
hg38428614
hg19481385
hg18481385
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5971n100
Supporting Variantsnssv3657533
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)nsv1016305
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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