A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6383873



Internal ID21041426
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 StatusM
Merged Variants
Supporting Variantsnssv18211348
Samples
Known GenesNDST3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6383873
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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