A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6376028



Internal ID21033581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:115979296..116212097hg38UCSC Ensembl
chr4:116900452..117133253hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38232802
hg19232802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18107177
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6376028
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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