A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5429418



Internal ID208267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:140763458..140763520hg38UCSC Ensembl
chrX:139845623..139845685hg19UCSC Ensembl
CytobandXq27.1
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17742702
Samples
Known GenesLINC00632
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5429418
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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