A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17739761



Internal ID163427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:24995849..24999810hg38UCSC Ensembl
chrX:25013966..25017927hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg383962
hg193962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5432765
Supporting Variants
Samples
Known GenesPOLA1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17739761
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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