A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515438



Internal ID20888798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:19478680..19483225hg38UCSC Ensembl
chr17:19381993..19386538hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg384546
hg194546
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18034792
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515438
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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