A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv995924



Internal ID15943194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:38664098..38665115hg38UCSC Ensembl
Innerchr4:38665719..38666736hg19UCSC Ensembl
Innerchr4:38342114..38343131hg18UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg381018
hg191018
hg181018
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv594005
Supporting Variants
Samples
Known GenesFLJ13197, KLF3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv995924
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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