A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6530315



Internal ID20903676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:17265105..17266951hg38UCSC Ensembl
chr19:17375914..17377760hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg381847
hg191847
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197691
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6530315
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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