A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6495727



Internal ID20868921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:39305979..39316904hg38UCSC Ensembl
chr17:37462232..37473157hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3810926
hg1910926
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18035343
Samples
Known GenesFBXL20
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6495727
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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