A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18198298



Internal ID20765338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:51168346..51212096hg38UCSC Ensembl
chr19:51671603..51715352hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3843751
hg1943750
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6532706
Supporting Variants
Samples
Known GenesMIR8074, SIGLEC17P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18198298
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00013


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