A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6368267



Internal ID21025820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:11260883..11276002hg38UCSC Ensembl
chr4:11262507..11277626hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3815120
hg1915120
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209553
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6368267
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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