A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604564



Internal ID16391973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:120046039..120315152hg38UCSC Ensembl
Innerchr6:120367185..120636298hg19UCSC Ensembl
Innerchr6:120408884..120677997hg18UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg38269114
hg19269114
hg18269114
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1072354
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604564
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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