A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6475308



Internal ID21132861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:56863747..56885752hg38UCSC Ensembl
chr12:57257531..57279536hg19UCSC Ensembl
Cytoband12q13.3
Allele length
AssemblyAllele length
hg3822006
hg1922006
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18177396
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6475308
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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