A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18214376



Internal ID20781416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:9701671..10217414hg38UCSC Ensembl
chr4:9703295..10219038hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38515744
hg19515744
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6368350
Supporting Variants
Samples
Known GenesDRD5, MIR3138, SLC2A9, WDR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18214376
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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