A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6386136



Internal ID21043689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:43887479..43888258hg38UCSC Ensembl
chr5:43887581..43888360hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg38780
hg19780
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18132710
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6386136
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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