A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436109



Internal ID21093662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:26571335..26657745hg38UCSC Ensembl
chr10:26860264..26946674hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3886411
hg1986411
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18177584
Samples
Known GenesLINC00202-2, LINC00264
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436109
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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