A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6506093



Internal ID20879368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:13234168..13234614hg38UCSC Ensembl
chr17:13137485..13137931hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg38447
hg19447
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196863
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6506093
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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