A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6365803



Internal ID21023356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:131505815..131507261hg38UCSC Ensembl
chr3:131224659..131226105hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg381447
hg191447
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094268
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6365803
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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