A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6385162



Internal ID21042715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:170086801..170093900hg38UCSC Ensembl
chr4:171007952..171015051hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg387100
hg197100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213875
Samples
Known GenesAADAT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6385162
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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