A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv600809



Internal ID16388218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:1732507..1775202hg38UCSC Ensembl
Innerchr6:1732741..1775436hg19UCSC Ensembl
Innerchr6:1677740..1720435hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3842696
hg1942696
hg1842696
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1048588
Samples
Known GenesGMDS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv600809
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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