A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18229173



Internal ID20796213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:43461166..43475193hg38UCSC Ensembl
chr6:43428904..43442931hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3814028
hg1914028
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6399978
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18229173
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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