A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6137943



Internal ID337124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:153257953..153277153hg38UCSC Ensembl
chrX:152523414..152542610hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3819201
hg1919197
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17738063
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6137943
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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