A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6397155



Internal ID21054708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:61274767..61289803hg38UCSC Ensembl
chr5:60570594..60585630hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg3815037
hg1915037
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216253
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6397155
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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