A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6360615



Internal ID21018168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:13291071..13297868hg38UCSC Ensembl
chr3:13332571..13339368hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg386798
hg196798
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094200
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6360615
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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