A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6410131



Internal ID21067684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:141265520..141266465hg38UCSC Ensembl
chr5:140645088..140646033hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg38946
hg19946
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18125225
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6410131
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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