A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5975681



Internal ID22750616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:88291285..88299775hg38UCSC Ensembl
chrX:87546286..87554776hg19UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg388491
hg198491
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17516898
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5975681
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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