A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6490364



Internal ID21147917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:77725179..77725804hg38UCSC Ensembl
chr13:78299314..78299939hg19UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg38626
hg19626
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18013222
Samples
Known GenesSLAIN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6490364
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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