A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18220191



Internal ID20787231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:901727..909024hg38UCSC Ensembl
chr6:901735..909612hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg387298
hg197878
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6398533
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18220191
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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