A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6358118



Internal ID21015671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:35296426..35310343hg38UCSC Ensembl
chr4:35298048..35311965hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3813918
hg1913918
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213525
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6358118
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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