A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6413816



Internal ID21071369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:65917701..65944900hg38UCSC Ensembl
chr5:65213529..65240728hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg3827200
hg1927200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5778n223
Supporting Variantsnssv18214833
Samples
Known GenesERBB2IP, LOC100303749
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6413816
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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