A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18175910



Internal ID20742950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:20831773..20896895hg38UCSC Ensembl
chr9:20831772..20896894hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3865123
hg1965123
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6427007
Supporting Variants
Samples
Known GenesFOCAD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18175910
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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