A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13699265



Internal ID21221114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:12698690..12699025hg38UCSC Ensembl
chrUn_gl000235:6960..7295hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38336
hg19336
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2804344
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13699265
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.875


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