A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17739148



Internal ID162814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:8166634..8338432hg38UCSC Ensembl
chrX:8134675..8306473hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg38171799
hg19171799
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5423380
Supporting Variants
Samples
Known GenesVCX2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17739148
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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