A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv600779



Internal ID16041502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:383546..439985hg38UCSC Ensembl
Innerchr6:383546..439985hg19UCSC Ensembl
Innerchr6:328546..384985hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3856440
hg1956440
hg1856440
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1047588, nssv1047589
Samples
Known GenesIRF4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv600779
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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