A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6090187



Internal ID21999420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:59714039..59714039hg38UCSC Ensembl
chr17:57791400..57791400hg19UCSC Ensembl
Cytoband17q23.1
Allele length
AssemblyAllele length
hg382622
hg192622
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17618814
Samples
Known GenesVMP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6090187
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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