A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18185526



Internal ID20752566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:124935429..124936158hg38UCSC Ensembl
chr12:125419975..125420704hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg38730
hg19730
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6478011
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18185526
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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