A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13690726



Internal ID21212579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:239280931..239281027hg38UCSC Ensembl
chr2:240202627..240202723hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2806266
Supporting Variants
Samples
Known GenesHDAC4
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13690726
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.234375


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