A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6531932



Internal ID20905293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:14027520..14050277hg38UCSC Ensembl
chr19:14138332..14161089hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3822758
hg1922758
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197388
Samples
Known GenesIL27RA, RLN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6531932
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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