A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17515432



Internal ID22573393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:135534435..135549311hg38UCSC Ensembl
chrX:134668360..134683236hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg3814877
hg1914877
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5967869
Supporting Variants
Samples
Known GenesDDX26B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17515432
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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