A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5618594



Internal ID21566899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:134959695..134959695hg38UCSC Ensembl
chrX:134093725..134093725hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg38360
hg19360
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17165330, nssv17165331
SamplesHG01505, HG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5618594
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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