A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5430061



Internal ID208889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:149436276..149436336hg38UCSC Ensembl
chrX:148517807..148517867hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17737902
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5430061
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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