A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6491496



Internal ID21149049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:60691576..60692097hg38UCSC Ensembl
chr13:61265710..61266231hg19UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg38522
hg19522
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18010600
Samples
Known GenesLINC00378
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6491496
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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