A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5423083



Internal ID202109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:76903108..76924989hg38UCSC Ensembl
chrX:76123533..76145414hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg3821882
hg1921882
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv572n206
Supporting Variantsnssv17740866
Samples
Known GenesMIR384
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5423083
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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