A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552386



Internal ID20925513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:58500606..58501122hg38UCSC Ensembl
chr20:57075662..57076178hg19UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg38517
hg19517
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18069119
Samples
Known GenesAPCDD1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552386
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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