A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18102529



Internal ID20669569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:74360658..74361392hg38UCSC Ensembl
chr3:74409809..74410543hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38735
hg19735
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6368346
Supporting Variants
Samples
Known GenesCNTN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18102529
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00029


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