A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026271



Internal ID19115488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:1286348..1328788hg38UCSC Ensembl
Innerchr6:1286583..1329023hg19UCSC Ensembl
Innerchr6:1231583..1274023hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3842441
hg1942441
hg1842441
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5910n100
Supporting Variantsnssv3654717
Samples
Known GenesFOXQ1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026271
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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