A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6370509



Internal ID21028062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:141219575..141229837hg38UCSC Ensembl
chr3:140938417..140948679hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg3810263
hg1910263
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094295
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6370509
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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