A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737311



Internal ID160977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:119207425..119209149hg38UCSC Ensembl
chrX:118341388..118343112hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg381725
hg191725
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5415014
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737311
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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