A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6473103



Internal ID21130656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:10427919..10443397hg38UCSC Ensembl
chr12:10580518..10595996hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg3815479
hg1915479
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183142
Samples
Known GenesKLRC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6473103
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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