A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604568



Internal ID16391977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:120260579..120348840hg38UCSC Ensembl
Innerchr6:120581725..120669986hg19UCSC Ensembl
Innerchr6:120623424..120711685hg18UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3888262
hg1988262
hg1888262
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1072358
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604568
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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