A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18190032



Internal ID20757072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:86063128..86064396hg38UCSC Ensembl
chr9:88678043..88679311hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg381269
hg191269
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6436726
Supporting Variants
Samples
Known GenesGOLM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18190032
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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