A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6385669



Internal ID21043222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:72531001..72783100hg38UCSC Ensembl
chr4:73396718..73648817hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg38252100
hg19252100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211746
Samples
Known GenesADAMTS3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6385669
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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