A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18070610



Internal ID20637650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:7364501..7377700hg38UCSC Ensembl
chr20:7345148..7358347hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg3813200
hg1913200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6519952
Supporting Variants
Samples
Known GenesMIR8062
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18070610
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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