A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18188617



Internal ID20755657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:29027004..29062818hg38UCSC Ensembl
chr17:27354022..27389836hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3835815
hg1935815
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6498247
Supporting Variants
Samples
Known GenesPIPOX
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18188617
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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