A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6414791



Internal ID21072344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:163403337..163477662hg38UCSC Ensembl
chr5:162830343..162904668hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3874326
hg1974326
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215960
Samples
Known GenesCCNG1, HMMR, NUDCD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6414791
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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