A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13687027



Internal ID21208882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:118123827..118124710hg38UCSC Ensembl
chr2:118881403..118882286hg19UCSC Ensembl
Cytoband2q14.2
Allele length
AssemblyAllele length
hg38884
hg19884
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2804722
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13687027
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0625


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