A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5974331



Internal ID22749266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:63465555..63467254hg38UCSC Ensembl
chrX:62685435..62687134hg19UCSC Ensembl
CytobandXq11.1
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17516530
Samples
Known GenesLOC92249
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5974331
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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