A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6528078



Internal ID20901439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:65688201..65696400hg38UCSC Ensembl
chr17:63684319..63692518hg19UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg388200
hg198200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18037852
Samples
Known GenesCEP112
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6528078
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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