A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18039162



Internal ID20606202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:9700997..9701853hg38UCSC Ensembl
chr17:9604314..9605170hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg38857
hg19857
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6512845
Supporting Variants
Samples
Known GenesUSP43
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18039162
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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