A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5868368



Internal ID22643303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:6160960..6161401hg38UCSC Ensembl
chrX:6079001..6079442hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg38442
hg19442
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17456351
Samples
Known GenesNLGN4X
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5868368
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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