A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1047593



Internal ID15554093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:665448..667756hg38UCSC Ensembl
Innerchr6:665448..667756hg19UCSC Ensembl
Innerchr6:610448..612756hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg382309
hg192309
hg182309
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv600785
Supporting Variants
Samples
Known GenesEXOC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1047593
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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