A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18175066



Internal ID20742106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:114594801..114596900hg38UCSC Ensembl
chr9:117357081..117359180hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6440522
Supporting Variants
Samples
Known GenesATP6V1G1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18175066
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00026


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