A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5431367



Internal ID210145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:75673010..75673280hg38UCSC Ensembl
chrX:74892845..74893115hg19UCSC Ensembl
CytobandXq13.3
Allele length
AssemblyAllele length
hg38271
hg19271
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17740807
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5431367
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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