A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5609774



Internal ID21558079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:45121761..45121761hg38UCSC Ensembl
chrX:44981006..44981006hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg381149
hg191149
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17167987
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5609774
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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