A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6517068



Internal ID20890429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:2122553..2127194hg38UCSC Ensembl
chr20:2103199..2107840hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg384642
hg194642
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18067084
Samples
Known GenesSTK35
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6517068
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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