A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526345



Internal ID20899706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:65636578..65807634hg38UCSC Ensembl
chr17:63632696..63803752hg19UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg38171057
hg19171057
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18037846
Samples
Known GenesCEP112
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526345
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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