A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6412409



Internal ID21069962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:58551554..58554309hg38UCSC Ensembl
chr5:57847381..57850136hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg382756
hg192756
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18133678
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6412409
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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