A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17736512



Internal ID160178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:40512082..40516306hg38UCSC Ensembl
chrX:40371334..40375558hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg384225
hg194225
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5415895
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17736512
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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