A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13683056



Internal ID21204913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:43975870..43975983hg38UCSC Ensembl
chr17:42053238..42053351hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38114
hg19114
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2797791
Supporting Variants
Samples
Known GenesPYY
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13683056
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.859375


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