A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6470895



Internal ID21128448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:94982559..94985351hg38UCSC Ensembl
chr12:95376335..95379127hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg382793
hg192793
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18005848
Samples
Known GenesNDUFA12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6470895
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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