A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6479582



Internal ID21137135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:46339021..46449695hg38UCSC Ensembl
chr14:46808224..46918898hg19UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg38110675
hg19110675
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18192347
Samples
Known GenesLINC00871
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6479582
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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