A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6451108



Internal ID21108661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:131604180..131867172hg38UCSC Ensembl
chr10:133436516..133677527hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38262993
hg19241012
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182165
Samples
Known GenesFLJ46300
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6451108
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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