A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6413826



Internal ID21071379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:134628095..134629653hg38UCSC Ensembl
chr5:133963785..133965343hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg381559
hg191559
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214483
Samples
Known GenesSAR1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6413826
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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