A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18211348



Internal ID20778388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:118011401..118053100hg38UCSC Ensembl
chr4:118932556..118974255hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg3841700
hg1941700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6383873
Supporting Variants
Samples
Known GenesNDST3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18211348
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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