A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17742653



Internal ID166319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:139449663..139555260hg38UCSC Ensembl
chrX:138531822..138637419hg19UCSC Ensembl
CytobandXq27.1
Allele length
AssemblyAllele length
hg38105598
hg19105598
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5424853
Supporting Variants
Samples
Known GenesF9
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17742653
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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