A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6475910



Internal ID21133463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:20919415..20955547hg38UCSC Ensembl
chr14:21387574..21423706hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3836133
hg1936133
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2049n223
Supporting Variantsnssv18186117
Samples
Known GenesECRP, RNASE2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6475910
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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