A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6087508



Internal ID21996741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119261073..119261073hg38UCSC Ensembl
chr10:121020585..121020585hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg38118
hg19118
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17590245
Samples
Known GenesGRK5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6087508
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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