A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138019



Internal ID337201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:84236542..84253000hg38UCSC Ensembl
chrX:83491550..83508008hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg3816459
hg1916459
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv574n206
Supporting Variantsnssv17741125
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138019
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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