A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18102832



Internal ID20669872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:56432928..56434277hg38UCSC Ensembl
chr3:56466956..56468305hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg381350
hg191350
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6363392
Supporting Variants
Samples
Known GenesERC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18102832
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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