A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv916094



Internal ID16210050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:113047167..113052485hg38UCSC Ensembl
Innerchr2:113804744..113810062hg19UCSC Ensembl
Innerchr2:113521215..113526533hg18UCSC Ensembl
Cytoband2q13
Allele length
AssemblyAllele length
hg385319
hg195319
hg185319
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv582709
Supporting Variants
Samples
Known GenesIL36B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv916094
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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