A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6518433



Internal ID20891794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:81525114..81529056hg38UCSC Ensembl
chr17:79492140..79496082hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg383943
hg193943
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18038558
Samples
Known GenesFSCN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6518433
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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