A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv600780



Internal ID16388189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:403799..442410hg38UCSC Ensembl
Innerchr6:403799..442410hg19UCSC Ensembl
Innerchr6:348799..387410hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3838612
hg1938612
hg1838612
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1153395
Samples1780862093_A
Known GenesIRF4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv600780
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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