A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1092076



Internal ID15598576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:104303789..104388960hg38UCSC Ensembl
Innerchr7:103944237..104029408hg19UCSC Ensembl
Innerchr7:103731473..103816644hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3885172
hg1985172
hg1885172
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv608067
Supporting Variants
Samples
Known GenesLHFPL3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1092076
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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