A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6476174



Internal ID21133727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:112393848..112398568hg38UCSC Ensembl
chr13:113048162..113052882hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg384721
hg194721
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195064
Samples
Known GenesSPACA7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6476174
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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