A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18175004



Internal ID20742044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:14876596..14976321hg38UCSC Ensembl
chr9:14876594..14976319hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3899726
hg1999726
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6429996
Supporting Variants
Samples
Known GenesFREM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18175004
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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