A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6317078



Internal ID20850162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:20510700..20512911hg38UCSC Ensembl
chr1:20837193..20839404hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg382212
hg192212
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18201858
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6317078
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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