A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019761



Internal ID19108979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167183745..167239395hg38UCSC Ensembl
Innerchr6:167597233..167652883hg19UCSC Ensembl
Innerchr6:167517223..167572873hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3855651
hg1955651
hg1855651
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3655402
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)nsv1019761
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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