A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138291



Internal ID337475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:76510542..76621600hg38UCSC Ensembl
chrX:75730955..75842009hg19UCSC Ensembl
CytobandXq13.3
Allele length
AssemblyAllele length
hg38111059
hg19111055
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17740845
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138291
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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