A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6522096



Internal ID20895457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:77458596..77460469hg38UCSC Ensembl
chr17:75454678..75456551hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg381874
hg191874
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18039006
Samples
Known GenesSEPT9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6522096
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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