A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13703216



Internal ID21225029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:112776416..112776599hg38UCSC Ensembl
chr2:113533993..113534176hg19UCSC Ensembl
Cytoband2q13
Allele length
AssemblyAllele length
hg38184
hg19184
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2805127
Supporting Variants
Samples
Known GenesIL1A
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13703216
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency1


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