A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6390908



Internal ID21048461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:116379782..116615768hg38UCSC Ensembl
chr4:117300938..117536924hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38235987
hg19235987
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211324
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6390908
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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