A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18204293



Internal ID20771333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:6520417..6587903hg38UCSC Ensembl
chr1:6580477..6647963hg19UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg3867487
hg1967487
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6329098
Supporting Variants
Samples
Known GenesNOL9, TAS1R1, ZBTB48
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18204293
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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