A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17736943



Internal ID160609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:51246100..51265600hg38UCSC Ensembl
chrX:50988933..51008463hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg3819501
hg1919531
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5433329
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17736943
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000627221


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