A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027208



Internal ID19116427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:149649..253272hg38UCSC Ensembl
Innerchr6:149649..253272hg19UCSC Ensembl
Innerchr6:94649..198272hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38103624
hg19103624
hg18103624
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5867n100
Supporting Variantsnssv3650367
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)nsv1027208
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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