A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737508



Internal ID161174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:123925709..123933254hg38UCSC Ensembl
chrX:123059559..123067104hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg387546
hg197546
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5416575
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737508
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00208117


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