A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6389364



Internal ID21046917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:94757301..94759400hg38UCSC Ensembl
chr4:95678452..95680551hg19UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215401
Samples
Known GenesBMPR1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6389364
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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