A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6477944



Internal ID21135497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:108259729..108260169hg38UCSC Ensembl
chr12:108653506..108653946hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg38441
hg19441
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17996201
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6477944
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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