A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737531



Internal ID161197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:128912308..128912423hg38UCSC Ensembl
chrX:128046286..128046401hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5415659
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737531
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001561


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