A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17742392



Internal ID166058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:132866800..132881500hg38UCSC Ensembl
chrX:132000828..132015528hg19UCSC Ensembl
CytobandXq26.2
Allele length
AssemblyAllele length
hg3814701
hg1914701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5414017
Supporting Variants
Samples
Known GenesHS6ST2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17742392
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00250784


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