A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6465726



Internal ID21123279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:84455877..84584831hg38UCSC Ensembl
chr12:84849656..84978610hg19UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg38128955
hg19128955
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180186
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6465726
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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