A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526302



Internal ID20899663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:78530399..78532842hg38UCSC Ensembl
chr17:76526481..76528924hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg382444
hg192444
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18038109
Samples
Known GenesDNAH17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526302
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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