A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6476306



Internal ID21133859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:50664734..50689139hg38UCSC Ensembl
chr14:51131452..51155857hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg3824406
hg1924406
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196306
Samples
Known GenesSAV1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6476306
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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