A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6360735



Internal ID21018288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:8512956..8528178hg38UCSC Ensembl
chr4:8514683..8529905hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3815223
hg1915223
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214740
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6360735
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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