A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6474347



Internal ID21131900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:78061301..78062700hg38UCSC Ensembl
chr12:78455081..78456480hg19UCSC Ensembl
Cytoband12q21.2
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18004518
Samples
Known GenesNAV3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6474347
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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