A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18196676



Internal ID20763716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:15862101..15886700hg38UCSC Ensembl
chr12:16015035..16039634hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg3824600
hg1924600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6460395
Supporting Variants
Samples
Known GenesSTRAP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18196676
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00015


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