A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1091882



Internal ID15945068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:100991862..101004836hg38UCSC Ensembl
Innerchr7:100635143..100648117hg19UCSC Ensembl
Innerchr7:100421863..100434837hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3812975
hg1912975
hg1812975
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv607971
Supporting Variants
Samples
Known GenesMUC12
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1091882
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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