A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17739172



Internal ID162838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:8871218..8889475hg38UCSC Ensembl
chrX:8839259..8857516hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg3818258
hg1918258
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5433716
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17739172
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00312175


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