A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5427257



Internal ID206164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:19888000..19888347hg38UCSC Ensembl
chrX:19906118..19906465hg19UCSC Ensembl
CytobandXp22.12
Allele length
AssemblyAllele length
hg38348
hg19348
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17739545
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5427257
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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