A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18180898



Internal ID20747938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:52435965..52456764hg38UCSC Ensembl
chr12:52829749..52850548hg19UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg3820800
hg1920800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6463772
Supporting Variants
Samples
Known GenesKRT6B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18180898
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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