A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515767



Internal ID20889128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:38276054..38323179hg38UCSC Ensembl
chr19:38766694..38813819hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3847126
hg1947126
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198100
Samples
Known GenesC19orf33, KCNK6, SPINT2, YIF1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515767
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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