A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608406



Internal ID16049129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:128837493..128856742hg38UCSC Ensembl
Innerchr7:128477547..128496796hg19UCSC Ensembl
Innerchr7:128264783..128284032hg18UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg3819250
hg1919250
hg1819250
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11613n54
Supporting Variantsnssv1094504
Samples
Known GenesFLNC
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608406
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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