A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6413208



Internal ID21070761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:132369401..132369900hg38UCSC Ensembl
chr5:131705093..131705592hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18127121
Samples
Known GenesLOC553103, SLC22A5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6413208
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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