A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5979269



Internal ID22754204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:75553924..75560486hg38UCSC Ensembl
chrX:74773759..74780321hg19UCSC Ensembl
CytobandXq13.3
Allele length
AssemblyAllele length
hg386563
hg196563
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17516729, nssv17516728
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5979269
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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