A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5967869



Internal ID22742804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:135534435..135549311hg38UCSC Ensembl
chrX:134668360..134683236hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg3814877
hg1914877
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17515432
Samples
Known GenesDDX26B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5967869
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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