A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6470773



Internal ID21128326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:103073563..103074018hg38UCSC Ensembl
chr12:103467341..103467796hg19UCSC Ensembl
Cytoband12q23.2
Allele length
AssemblyAllele length
hg38456
hg19456
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17995624
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6470773
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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