A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604453



Internal ID16391862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:107114862..107115612hg38UCSC Ensembl
Innerchr6:107436066..107436816hg19UCSC Ensembl
Innerchr6:107542759..107543509hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38751
hg19751
hg18751
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10898n54
Supporting Variantsnssv1071905
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604453
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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