A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6524545



Internal ID20897906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:38087393..38229833hg38UCSC Ensembl
chr20:36715795..36858235hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38142441
hg19142441
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202234
Samples
Known GenesKIAA1755, RPRD1B, TGM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6524545
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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