A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6488301



Internal ID21145854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:77980983..77981708hg38UCSC Ensembl
chr13:78555118..78555843hg19UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg38726
hg19726
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18012967
Samples
Known GenesLINC01069
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6488301
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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