A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6400079



Internal ID21057632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:52230740..52231203hg38UCSC Ensembl
chr5:51526574..51527037hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38464
hg19464
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18133540
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6400079
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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