A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv995863



Internal ID16289819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:36905679..36929802hg38UCSC Ensembl
Innerchr4:36907301..36931424hg19UCSC Ensembl
Innerchr4:36583696..36607819hg18UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3824124
hg1924124
hg1824124
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593987
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv995863
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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