A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6477967



Internal ID21135520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:120309558..120313707hg38UCSC Ensembl
chr12:120747361..120751510hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg384150
hg194150
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17997435
Samples
Known GenesSIRT4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6477967
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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