A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6386412



Internal ID21043965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:95167613..95168234hg38UCSC Ensembl
chr4:96088764..96089385hg19UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg38622
hg19622
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18121848
Samples
Known GenesUNC5C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6386412
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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