A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6492805



Internal ID21150358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:126389353..126747623hg38UCSC Ensembl
chr12:126873899..127232169hg19UCSC Ensembl
Cytoband12q24.32
Allele length
AssemblyAllele length
hg38358271
hg19358271
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1727n223
Supporting Variantsnssv18186076
Samples
Known GenesLINC00943, LINC00944, LOC100128554
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6492805
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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