A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17736996



Internal ID160662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:52630932..52686964hg38UCSC Ensembl
chrX:52659982..52716014hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg3856033
hg1956033
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5432894
Supporting Variants
Samples
Known GenesSSX7, SSX8
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17736996
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00900524


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