A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138351



Internal ID337535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:2201873..2403011hg38UCSC Ensembl
chrX:2119849..2321052hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg38201139
hg19201204
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17738970
Samples
Known GenesDHRSX
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138351
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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