A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203426



Internal ID20770466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:62943848..62973196hg38UCSC Ensembl
chr20:61575200..61604548hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3829349
hg1929349
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6551088
Supporting Variants
Samples
Known GenesGID8, SLC17A9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203426
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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