A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6088496



Internal ID21997729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:48706218..48706218hg38UCSC Ensembl
chr10:49914263..49914263hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg38258
hg19258
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17584514
Samples
Known GenesWDFY4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6088496
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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