A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6369890



Internal ID21027443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:16837020..16881077hg38UCSC Ensembl
chr4:16838643..16882700hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg3844058
hg1944058
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18115341
Samples
Known GenesLDB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6369890
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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