A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6524129



Internal ID20897490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:31891401..31893200hg38UCSC Ensembl
chr20:30479204..30481003hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203265
Samples
Known GenesTTLL9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6524129
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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