A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17736997



Internal ID160663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:52644700..52670964hg38UCSC Ensembl
chrX:52673750..52700014hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg3826265
hg1926265
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5421384
Supporting Variants
Samples
Known GenesSSX7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17736997
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000209161


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