A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6386010



Internal ID21043563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:107904787..107916715hg38UCSC Ensembl
chr4:108825943..108837871hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3811929
hg1911929
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209504
Samples
Known GenesSGMS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6386010
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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