A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6459100



Internal ID21116653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:64260529..64265327hg38UCSC Ensembl
chr12:64654309..64659107hg19UCSC Ensembl
Cytoband12q14.2
Allele length
AssemblyAllele length
hg384799
hg194799
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18002856
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6459100
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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