A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182182



Internal ID20749222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:8254701..8339300hg38UCSC Ensembl
chr12:8407297..8491896hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg3884600
hg1984600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6472080
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182182
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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