A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18202460



Internal ID20769500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:37752101..37754500hg38UCSC Ensembl
chr1:38217773..38220172hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg382400
hg192400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6331720
Supporting Variants
Samples
Known GenesEPHA10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18202460
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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