A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6477984



Internal ID21135537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:36074048..36091187hg38UCSC Ensembl
chr14:36543254..36560393hg19UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg3817140
hg1917140
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193326
Samples
Known GenesLINC00609
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6477984
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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