A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18197675



Internal ID20764715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:16693938..16730277hg38UCSC Ensembl
chr19:16804749..16841088hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg3836340
hg1936340
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6521338
Supporting Variants
Samples
Known GenesNWD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18197675
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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