A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6494777



Internal ID21152330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:120296360..120318251hg38UCSC Ensembl
chr12:120734163..120756054hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg3821892
hg1921892
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17997431
Samples
Known GenesSIRT4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6494777
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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