A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6375345



Internal ID21032898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:3113487..3122630hg38UCSC Ensembl
chr3:3155171..3164314hg19UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg389144
hg199144
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18099316
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6375345
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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