A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18216156



Internal ID20783196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:1741537..1791246hg38UCSC Ensembl
chr6:1741771..1791480hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3849710
hg1949710
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6401486
Supporting Variants
Samples
Known GenesGMDS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18216156
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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