A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6377995



Internal ID21035548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:170682621..170697498hg38UCSC Ensembl
chr4:171603772..171618649hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg3814878
hg1914878
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213882
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6377995
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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