A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17736592



Internal ID160258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:42062160..42062222hg38UCSC Ensembl
chrX:41921413..41921475hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5416394
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17736592
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.002029


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