A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18227340



Internal ID20794380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:60276601..60283500hg38UCSC Ensembl
chr8:61189160..61196059hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg386900
hg196900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6415894
Supporting Variants
Samples
Known GenesCA8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18227340
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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