A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6366134



Internal ID21023687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:74389109..74390150hg38UCSC Ensembl
chr3:74438260..74439301hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg381042
hg191042
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18102530
Samples
Known GenesCNTN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6366134
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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