A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5431013



Internal ID209802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:86225271..86225505hg38UCSC Ensembl
chrX:85480274..85480508hg19UCSC Ensembl
CytobandXq21.2
Allele length
AssemblyAllele length
hg38235
hg19235
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17741213
Samples
Known GenesDACH2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5431013
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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