A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5979856



Internal ID22754791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:119393006..119403037hg38UCSC Ensembl
chrX:118526969..118537000hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg3810032
hg1910032
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17515255
Samples
Known GenesSLC25A43
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5979856
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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