A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532893



Internal ID20906254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:36673946..36678430hg38UCSC Ensembl
chr20:35302349..35306833hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg384485
hg194485
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18068063
Samples
Known GenesNDRG3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6532893
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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