A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6456093



Internal ID21113646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:95741536..95744272hg38UCSC Ensembl
chr12:96135314..96138050hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg382737
hg192737
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18005878
Samples
Known GenesNTN4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6456093
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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