A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608067



Internal ID16048790
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 StatusM
Merged Variants
Supporting Variantsnssv1092076
Samples
Known GenesLHFPL3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608067
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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