A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18227785



Internal ID20794825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:95787408..95833881hg38UCSC Ensembl
chr6:96235284..96281757hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg3846474
hg1946474
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6412079
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18227785
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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