A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17740880



Internal ID164546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:77590239..77593539hg38UCSC Ensembl
chrX:76845709..76849009hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg383301
hg193301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5428426
Supporting Variants
Samples
Known GenesATRX
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17740880
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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