A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18212070



Internal ID20779110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:150255578..150258371hg38UCSC Ensembl
chr4:151176730..151179523hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg382794
hg192794
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6379585
Supporting Variants
Samples
Known GenesDCLK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18212070
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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