A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6491247



Internal ID21148800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:46017574..46018165hg38UCSC Ensembl
chr13:46591709..46592300hg19UCSC Ensembl
Cytoband13q14.13
Allele length
AssemblyAllele length
hg38592
hg19592
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18009824
Samples
Known GenesZC3H13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6491247
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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