A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6407236



Internal ID21064789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:55161701..55260700hg38UCSC Ensembl
chr5:54457529..54556528hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3899000
hg1999000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214044
Samples
Known GenesCCNO, CDC20B, DHX29, GPX8, MCIDAS, MIR449A, MIR449B, MIR449C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6407236
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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