A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6381237



Internal ID21038790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:115600836..115601231hg38UCSC Ensembl
chr4:116521992..116522387hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38396
hg19396
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18107110
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6381237
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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