A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6488926



Internal ID21146479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113126355..113128715hg38UCSC Ensembl
chr13:113780669..113783029hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg382361
hg192361
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18007311
Samples
Known GenesF10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6488926
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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