A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607979



Internal ID16395388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:101325082..101386149hg38UCSC Ensembl
Innerchr7:100968363..101029430hg19UCSC Ensembl
Innerchr7:100755083..100816150hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3861068
hg1961068
hg1861068
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1091890
Samples
Known GenesCOL26A1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607979
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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