A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18186708



Internal ID20753748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:81837812..81878743hg38UCSC Ensembl
chr12:82231591..82272522hg19UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg3840932
hg1940932
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6470402
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18186708
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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