A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6487227



Internal ID21144780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:51379565..51380407hg38UCSC Ensembl
chr13:51953701..51954543hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg38843
hg19843
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18009668
Samples
Known GenesINTS6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6487227
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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