A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6391609



Internal ID21049162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:139015301..139017500hg38UCSC Ensembl
chr4:139936455..139938654hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213029
Samples
Known GenesCCRN4L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6391609
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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