A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6005369



Internal ID21914712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:56342093..56498252hg38UCSC Ensembl
chr10:58101854..58258013hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38156160
hg19156160
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17584577
Samples
Known GenesZWINT
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6005369
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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