A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6380928



Internal ID21038481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:94936363..94942442hg38UCSC Ensembl
chr4:95857514..95863593hg19UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg386080
hg196080
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18121834
Samples
Known GenesBMPR1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6380928
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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