A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5972025



Internal ID22746960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:117758969..117779384hg38UCSC Ensembl
chrX:116892932..116913347hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg3820416
hg1920416
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17515221
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5972025
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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