A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13677399



Internal ID21199252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:100270772..100270772hg38UCSC Ensembl
chr15:100810977..100810977hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2794128
Supporting Variants
Samples
Known GenesADAMTS17
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13677399
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.546875


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