A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6437471



Internal ID21095024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:126751656..127097635hg38UCSC Ensembl
chr10:128440225..128895899hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg38345980
hg19455675
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195431
Samples
Known GenesDOCK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6437471
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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