A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18214585



Internal ID20781626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:121678401..121690100hg38UCSC Ensembl
chr6:121999547..122011246hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3811700
hg1911700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6618526
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18214585
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00038


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