A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18234268



Internal ID20801308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:82824901..82857300hg38UCSC Ensembl
chr6:83534620..83567019hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3832400
hg1932400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6401284
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18234268
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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