A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6482243



Internal ID21139796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:29702862..29703288hg38UCSC Ensembl
chr13:30276999..30277425hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg38427
hg19427
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18007865
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6482243
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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