A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6461866



Internal ID21119419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:51174957..51179091hg38UCSC Ensembl
chr12:51568740..51572874hg19UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg384135
hg194135
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18192217
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6461866
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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