A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18185275



Internal ID20752315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:9844967..9894173hg38UCSC Ensembl
chr12:9997566..10046772hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg3849207
hg1949207
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6459368
Supporting Variants
Samples
Known GenesCLEC2B, KLRF1, KLRF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18185275
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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