A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737522



Internal ID161188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:128582263..128623652hg38UCSC Ensembl
chrX:127716241..127757630hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg3841390
hg1941390
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5432049
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737522
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00228928


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