A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5881726



Internal ID22656702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:97926417..99670485hg38UCSC Ensembl
chrX:97181415..98925483hg19UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg381744069
hg191744069
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17461732
Samples
Known GenesXRCC6P5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5881726
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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