A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6362349



Internal ID21019902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:71988303..71998986hg38UCSC Ensembl
chr3:72037454..72048137hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg3810684
hg1910684
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18103773
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6362349
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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