A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138259



Internal ID337443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:120481566..120506200hg38UCSC Ensembl
chrX:119615421..119640055hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg3824635
hg1924635
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17737384
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138259
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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