A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6442887



Internal ID21100440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:72411..199467hg38UCSC Ensembl
chr10:118351..245407hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38127057
hg19127057
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv595n223
Supporting Variantsnssv18191253
Samples
Known GenesZMYND11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6442887
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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