A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6484251



Internal ID21141804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:35442781..35443347hg38UCSC Ensembl
chr13:36016918..36017484hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38567
hg19567
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18008334
Samples
Known GenesNBEA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6484251
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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