A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5432972



Internal ID211701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:30658541..30659914hg38UCSC Ensembl
chrX:30676658..30678031hg19UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg381374
hg191374
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17736418
Samples
Known GenesGK
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5432972
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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