A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6374952



Internal ID21032505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:35026001..35056500hg38UCSC Ensembl
chr4:35027623..35058122hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3830500
hg1930500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5228n223
Supporting Variantsnssv18213521
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6374952
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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