A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6479978



Internal ID21137531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:88160652..88161103hg38UCSC Ensembl
chr13:88812907..88813358hg19UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg38452
hg19452
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18014970
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6479978
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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