A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18197287



Internal ID20764327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:30374401..30376900hg38UCSC Ensembl
chr19:30865308..30867807hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg382500
hg192500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6527137
Supporting Variants
Samples
Known GenesZNF536
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18197287
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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