A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13679243



Internal ID21201104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90819209..90819349hg38UCSC Ensembl
chr15:91362439..91362579hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38141
hg19141
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2794659
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13679243
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.40625


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