A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13676895



Internal ID21198748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:28516150..28517445hg38UCSC Ensembl
chr17:26843168..26844463hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg381296
hg191296
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2797349
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13676895
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.078125


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