A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6476224



Internal ID21133777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:116865459..116866090hg38UCSC Ensembl
chr12:117303264..117303895hg19UCSC Ensembl
Cytoband12q24.22
Allele length
AssemblyAllele length
hg38632
hg19632
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17997171
Samples
Known GenesHRK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6476224
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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