A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138903



Internal ID338087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:97349463..97369442hg38UCSC Ensembl
chrX:96604462..96624441hg19UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg3819980
hg1919980
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17737094
Samples
Known GenesDIAPH2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138903
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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