A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18214770



Internal ID20781810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:88275901..88330600hg38UCSC Ensembl
chr4:89197053..89251752hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3854700
hg1954700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6376368
Supporting Variants
Samples
Known GenesPPM1K
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18214770
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00048


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