A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1094509



Internal ID15601009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:128853335..128859025hg38UCSC Ensembl
Innerchr7:128493389..128499079hg19UCSC Ensembl
Innerchr7:128280625..128286315hg18UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg385691
hg195691
hg185691
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv608411
Supporting Variants
Samples
Known GenesFLNC
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1094509
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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