A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18214621



Internal ID20781662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:171494201..171596000hg38UCSC Ensembl
chr4:172415352..172517151hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg38101800
hg19101800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6381883
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18214621
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00021


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