A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6409280



Internal ID21066833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:91835072..91835647hg38UCSC Ensembl
chr5:91130889..91131464hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38576
hg19576
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18135556
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6409280
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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