A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17739617



Internal ID163283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:22211140..22211763hg38UCSC Ensembl
chrX:22229257..22229880hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg38624
hg19624
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5422693
Supporting Variants
Samples
Known GenesPHEX
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17739617
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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