A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6361206



Internal ID21018759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:150597056..150598353hg38UCSC Ensembl
chr3:150314843..150316140hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg381298
hg191298
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18096577
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6361206
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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