A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032802



Internal ID19122024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:149649..196357hg38UCSC Ensembl
Innerchr6:149649..196357hg19UCSC Ensembl
Innerchr6:94649..141357hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3846709
hg1946709
hg1846709
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5865n100
Supporting Variantsnssv3650361
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)nsv1032802
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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