A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6488563



Internal ID21146116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:110995088..110998710hg38UCSC Ensembl
chr12:111432892..111436514hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg383623
hg193623
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17996953
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6488563
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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