A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6547580



Internal ID20920781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:56365905..56366003hg38UCSC Ensembl
chr20:54940961..54941059hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18070410
Samples
Known GenesFAM210B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6547580
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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