A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019703



Internal ID19108921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:164003651..164067748hg38UCSC Ensembl
Innerchr6:164424683..164488780hg19UCSC Ensembl
Innerchr6:164344673..164408770hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3864098
hg1964098
hg1864098
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3749614
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)nsv1019703
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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