A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6391867



Internal ID21049420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:27485739..27520921hg38UCSC Ensembl
chr5:27485846..27521028hg19UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg3835183
hg1935183
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18129963
Samples
Known GenesLINC01021
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6391867
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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