A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18211645



Internal ID20778685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:68815701..68852200hg38UCSC Ensembl
chr4:69681419..69717918hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3836500
hg1936500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6393096
Supporting Variants
Samples
Known GenesUGT2B10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18211645
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0013


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