A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5424667



Internal ID203649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:23711051..23712132hg38UCSC Ensembl
chrX:23729168..23730249hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg381082
hg191082
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17739688
Samples
Known GenesACOT9
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5424667
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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