A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17741122



Internal ID164788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:84215738..84232989hg38UCSC Ensembl
chrX:83470746..83487997hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg3817252
hg1917252
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5429207
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17741122
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00291363


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