A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6481003



Internal ID21138556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:27360836..27368285hg38UCSC Ensembl
chr13:27934973..27942422hg19UCSC Ensembl
Cytoband13q12.2
Allele length
AssemblyAllele length
hg387450
hg197450
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18007499
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6481003
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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