A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6382207



Internal ID21039760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:84652905..84657181hg38UCSC Ensembl
chr4:85574058..85578334hg19UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg384277
hg194277
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214735
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6382207
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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