A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18196996



Internal ID20764036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:132987480..133379817hg38UCSC Ensembl
chr10:134800984..135193321hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38392338
hg19392338
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6443934
Supporting Variants
Samples
Known GenesADAM8, CALY, ECHS1, FUOM, GPR123, KNDC1, MIR202, MIR202HG, MIR3944, PAOX, PRAP1, TUBGCP2, UTF1, VENTX, ZNF511
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18196996
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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