A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6465000



Internal ID21122553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:93900382..93900974hg38UCSC Ensembl
chr12:94294158..94294750hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg38593
hg19593
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188343
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6465000
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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