A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016858



Internal ID19106075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:149649..229547hg38UCSC Ensembl
Innerchr6:149649..229547hg19UCSC Ensembl
Innerchr6:94649..174547hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3879899
hg1979899
hg1879899
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5866n100
Supporting Variantsnssv3650364
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)nsv1016858
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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