A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138896



Internal ID338080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:45349837..45355837hg38UCSC Ensembl
chrX:45209082..45215082hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg386001
hg196001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17736711
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138896
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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