A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6411774



Internal ID21069327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:52053570..52225597hg38UCSC Ensembl
chr5:51349404..51521431hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38172028
hg19172028
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18133513
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6411774
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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