A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6401013



Internal ID21058566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:145933323..145935879hg38UCSC Ensembl
chr5:145312886..145315442hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg382557
hg192557
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18126032
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6401013
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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