A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6491670



Internal ID21149223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:109861698..109869254hg38UCSC Ensembl
chr12:110299503..110307059hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg387557
hg197557
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178064
Samples
Known GenesGLTP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6491670
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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