A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5429304



Internal ID208154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:66165584..66165672hg38UCSC Ensembl
chrX:65385426..65385514hg19UCSC Ensembl
CytobandXq12
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17740419
Samples
Known GenesHEPH
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5429304
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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