A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604565



Internal ID16391974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:120068338..120163864hg38UCSC Ensembl
Innerchr6:120389484..120485010hg19UCSC Ensembl
Innerchr6:120431183..120526709hg18UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3895527
hg1995527
hg1895527
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1072355
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604565
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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