A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6466692



Internal ID21124245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:57246638..57248625hg38UCSC Ensembl
chr12:57640421..57642408hg19UCSC Ensembl
Cytoband12q13.3
Allele length
AssemblyAllele length
hg381988
hg191988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18001885
Samples
Known GenesSTAC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6466692
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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