A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6384971



Internal ID21042524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:77060501..77139500hg38UCSC Ensembl
chr4:77981654..78060653hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg3879000
hg1979000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212388
Samples
Known GenesCCNI
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6384971
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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