A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5975428



Internal ID22750363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:155692030..155699491hg38UCSC Ensembl
chrX:154921691..154929152hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg387462
hg197462
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17515756, nssv17515757
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5975428
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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