A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13686903



Internal ID21208761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:79840178..79840233hg38UCSC Ensembl
chr15:80132520..80132575hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2795297
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13686903
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.390625


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