A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv989306



Internal ID15936576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:4412889..4414085hg38UCSC Ensembl
Innerchr4:4414616..4415812hg19UCSC Ensembl
Innerchr4:4465517..4466713hg18UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg381197
hg191197
hg181197
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593477
Supporting Variants
Samples
Known GenesNSG1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv989306
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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