A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138885



Internal ID338069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:6064000..6176000hg38UCSC Ensembl
chrX:5982041..6094041hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg38112001
hg19112001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17736231
Samples
Known GenesNLGN4X
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138885
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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