A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv993062



Internal ID16287018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:11303292..11328451hg38UCSC Ensembl
Innerchr4:11304916..11330075hg19UCSC Ensembl
Innerchr4:10914014..10939173hg18UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg3825160
hg1925160
hg1825160
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593735
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)nssv993062
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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