A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6464229



Internal ID21121782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:11977744..11995592hg38UCSC Ensembl
chr12:12130678..12148526hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg3817849
hg1917849
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18181761
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6464229
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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