A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6531795



Internal ID20905156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:68891423..68897135hg38UCSC Ensembl
chr17:66887564..66893276hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg385713
hg195713
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18037565
Samples
Known GenesABCA8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6531795
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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