A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5429615



Internal ID208456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:56919021..56930414hg38UCSC Ensembl
chrX:56945454..56956847hg19UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg3811394
hg1911394
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17740279
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5429615
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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