A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18191376



Internal ID20758417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:95150334..95267598hg38UCSC Ensembl
chr12:95544110..95661374hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg38117265
hg19117265
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6460719
Supporting Variants
Samples
Known GenesFGD6, VEZT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18191376
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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