A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6373929



Internal ID21031482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:69510998..69525827hg38UCSC Ensembl
chr3:69560149..69574978hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3814830
hg1914830
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18104393
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6373929
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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