A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6525038



Internal ID20898399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:78763289..78776015hg38UCSC Ensembl
chr17:76759371..76772097hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3812727
hg1912727
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18038130
Samples
Known GenesCYTH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6525038
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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