A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5423347



Internal ID202368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:42815151..42815694hg38UCSC Ensembl
chrX:42674402..42674945hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg38544
hg19544
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17736610
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5423347
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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