A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6516562



Internal ID20889923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:78875291..78876797hg38UCSC Ensembl
chr17:76871373..76872879hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg381507
hg191507
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18038137
Samples
Known GenesTIMP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6516562
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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