A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6527334



Internal ID20900695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:31640908..31806706hg38UCSC Ensembl
chr19:32131814..32297612hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg38165799
hg19165799
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197299
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6527334
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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