A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5414671



Internal ID193942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:2437375..2438039hg38UCSC Ensembl
chrX:2355416..2356080hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg38665
hg19665
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17739002
Samples
Known GenesDHRSX
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5414671
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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