A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6402993



Internal ID21060546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:140721001..140728200hg38UCSC Ensembl
chr5:140100586..140107785hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg387200
hg197200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215096
Samples
Known GenesVTRNA1-3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6402993
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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