A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6491796



Internal ID21149349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:43688723..43689113hg38UCSC Ensembl
chr13:44262859..44263249hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg38391
hg19391
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18009088
Samples
Known GenesENOX1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6491796
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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