A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6473190



Internal ID21130743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:100862901..100864700hg38UCSC Ensembl
chr12:101256679..101258478hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17996714
Samples
Known GenesANO4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6473190
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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