A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6395259



Internal ID21052812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:45678915..45692918hg38UCSC Ensembl
chr4:45680932..45694935hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg3814004
hg1914004
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213693
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6395259
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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