A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5419910



Internal ID199030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:71160238..71161107hg38UCSC Ensembl
chrX:70380088..70380957hg19UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg38870
hg19870
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17740639
Samples
Known GenesNLGN3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5419910
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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