A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6096560



Internal ID22005793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:15050831..15050831hg38UCSC Ensembl
chr10:15092830..15092830hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38297
hg19297
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17596681
Samples
Known GenesOLAH
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6096560
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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