A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18094715



Internal ID20661755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:159625841..159638898hg38UCSC Ensembl
chr3:159343630..159356687hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg3813058
hg1913058
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6364355
Supporting Variants
Samples
Known GenesIQCJ-SCHIP1, SCHIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18094715
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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