A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6356188



Internal ID21013741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:3907402..4109080hg38UCSC Ensembl
chr3:3949086..4150764hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38201679
hg19201679
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4762n223
Supporting Variantsnssv18100867
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6356188
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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