A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6361659



Internal ID21019212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:24596336..24599861hg38UCSC Ensembl
chr4:24597959..24601484hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg383526
hg193526
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211785
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6361659
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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