A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138442



Internal ID337626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:53472964..53508964hg38UCSC Ensembl
chrX:53499916..53535930hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg3836001
hg1936015
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17737036
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138442
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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