A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6488636



Internal ID21146189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:111626402..111637329hg38UCSC Ensembl
chr12:112064206..112075133hg19UCSC Ensembl
Cytoband12q24.12
Allele length
AssemblyAllele length
hg3810928
hg1910928
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180498
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6488636
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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