A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5971239



Internal ID22746174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:9988556..9995053hg38UCSC Ensembl
chrX:9956596..9963093hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg386498
hg196498
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17517012
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5971239
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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