A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17742438



Internal ID166104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:134560135..134560887hg38UCSC Ensembl
chrX:133694165..133694917hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg38753
hg19753
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5433000
Supporting Variants
Samples
Known GenesLINC00629
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17742438
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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