A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6516687



Internal ID20890048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:37809013..37834496hg38UCSC Ensembl
chr19:38299653..38325136hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3825484
hg1925484
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198090
Samples
Known GenesLOC100631378, LOC644554
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6516687
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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