A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5615619



Internal ID21563924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:135012913..135012913hg38UCSC Ensembl
chrX:134146943..134146943hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17165332
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5615619
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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