A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17638687



Internal ID21830734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:24593432..24593488hg38UCSC Ensembl
chrX:24611549..24611605hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6105607
Supporting Variants
Samples
Known GenesPCYT1B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17638687
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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