A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6470516



Internal ID21128069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:97245063..97245918hg38UCSC Ensembl
chr12:97638841..97639696hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg38856
hg19856
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18006027
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6470516
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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