A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17741337



Internal ID165003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:88938542..88970542hg38UCSC Ensembl
chrX:88193543..88225543hg19UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg3832001
hg1932001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6138065
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17741337
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00293194


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