A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6378663



Internal ID21036216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:170846270..170846627hg38UCSC Ensembl
chr4:171767421..171767778hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg38358
hg19358
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18113455
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6378663
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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