A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6506354



Internal ID20879633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:19529044..19532896hg38UCSC Ensembl
chr17:19432357..19436209hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg383853
hg193853
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18034799
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6506354
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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