A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024769



Internal ID19113986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:102430788..102522015hg38UCSC Ensembl
Innerchr6:102878663..102969890hg19UCSC Ensembl
Innerchr6:102985356..103076583hg18UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3891228
hg1991228
hg1891228
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3649866
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)nsv1024769
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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