A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18096533



Internal ID20663573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:157555301..157559600hg38UCSC Ensembl
chr3:157273090..157277389hg19UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg384300
hg194300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6374503
Supporting Variants
Samples
Known GenesC3orf55
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18096533
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00015


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