A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18235111



Internal ID20802151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:27688307..27805373hg38UCSC Ensembl
chr6:27656086..27773151hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38117067
hg19117066
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6409158
Supporting Variants
Samples
Known GenesLINC01012, LOC100131289
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18235111
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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