A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6387398



Internal ID21044951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:48162873..48195319hg38UCSC Ensembl
chr4:48164890..48197336hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg3832447
hg1932447
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211881
Samples
Known GenesTEC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6387398
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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