A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5427280



Internal ID206187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:2571488..2577488hg38UCSC Ensembl
chrX:2489529..2495529hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg386001
hg196001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17739029
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5427280
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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