A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6377076



Internal ID21034629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:4141192..4146647hg38UCSC Ensembl
chr5:4141305..4146760hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg385456
hg195456
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18130983
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6377076
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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