A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18060996



Internal ID20628036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:34166335..34169674hg38UCSC Ensembl
chr1:34631936..34635275hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg383340
hg193340
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6321663
Supporting Variants
Samples
Known GenesC1orf94
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18060996
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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