A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6472467



Internal ID21130020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:95677408..95696080hg38UCSC Ensembl
chr12:96071184..96089856hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg3818673
hg1918673
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185628
Samples
Known GenesNTN4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6472467
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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