A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6403208



Internal ID21060761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:97868210..98078723hg38UCSC Ensembl
chr5:97203914..97414427hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38210514
hg19210514
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5830n223
Supporting Variantsnssv18136225
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6403208
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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