A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5424725



Internal ID203704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:32584889..32585016hg38UCSC Ensembl
chrX:32603006..32603133hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17739906
Samples
Known GenesDMD
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5424725
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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