A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5418881



Internal ID198037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:145136474..145227739hg38UCSC Ensembl
chrX:144217994..144309259hg19UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg3891266
hg1991266
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17737744
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5418881
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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