A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737026



Internal ID160692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:53289895..53291174hg38UCSC Ensembl
chrX:53319077..53320356hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg381280
hg191280
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5432441
Supporting Variants
Samples
Known GenesIQSEC2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737026
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000937


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