A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138352



Internal ID337536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:94698951..94704333hg38UCSC Ensembl
chrX:93953950..93959332hg19UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg385383
hg195383
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17741539
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138352
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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