A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496900



Internal ID20870103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:80058901..80060800hg38UCSC Ensembl
chr15:80351243..80353142hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184794
Samples
Known GenesZFAND6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496900
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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