A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737024



Internal ID160690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:53180970..53182031hg38UCSC Ensembl
chrX:53210152..53211213hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg381062
hg191062
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5422003
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737024
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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