A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18037582



Internal ID20604622
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 StatusS
Merged Variantsnsv6520091
Supporting Variants
Samples
Known GenesABCA9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18037582
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer