A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6531889



Internal ID20905250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:51577834..51591899hg38UCSC Ensembl
chr19:52081087..52095152hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3814066
hg1914066
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198305
Samples
Known GenesFLJ30403, ZNF175
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6531889
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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