A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5431090



Internal ID209875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:84652470..84653917hg38UCSC Ensembl
chrX:83907478..83908925hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg381448
hg191448
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17741145
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5431090
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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