A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6411736



Internal ID21069289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:77619801..77660600hg38UCSC Ensembl
chr5:76915626..76956425hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg3840800
hg1940800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216627
Samples
Known GenesOTP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6411736
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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