A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532617



Internal ID20905978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32121401..32123300hg38UCSC Ensembl
chr20:30709204..30711103hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203270
Samples
Known GenesTM9SF4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6532617
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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