A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6413228



Internal ID21070781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:56066831..56105390hg38UCSC Ensembl
chr5:55362658..55401217hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3838560
hg1938560
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214067
Samples
Known GenesANKRD55
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6413228
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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