A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5973543



Internal ID22748478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:57723484..57737257hg38UCSC Ensembl
chrX:57749917..57763690hg19UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg3813774
hg1913774
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17516467, nssv17516466, nssv17516468
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5973543
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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