A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6489053



Internal ID21146606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:117654547..117655966hg38UCSC Ensembl
chr12:118092352..118093771hg19UCSC Ensembl
Cytoband12q24.22
Allele length
AssemblyAllele length
hg381420
hg191420
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17997206
Samples
Known GenesKSR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6489053
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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