A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5425191



Internal ID204162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:131740437..131742309hg38UCSC Ensembl
chrX:130874465..130876337hg19UCSC Ensembl
CytobandXq26.2
Allele length
AssemblyAllele length
hg381873
hg191873
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17737622
Samples
Known GenesLOC286467
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5425191
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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