A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6520091



Internal ID20893452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:69010701..69024500hg38UCSC Ensembl
chr17:67006842..67020641hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3813800
hg1913800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18037582
Samples
Known GenesABCA9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6520091
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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