A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6139090



Internal ID338274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:24701724..24702001hg38UCSC Ensembl
chrX:24719841..24720118hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg38278
hg19278
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17739748
Samples
Known GenesPOLA1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6139090
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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