A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18185813



Internal ID20752853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:36134675..36148130hg38UCSC Ensembl
chr9:36134672..36148127hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3813456
hg1913456
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6449957
Supporting Variants
Samples
Known GenesGLIPR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18185813
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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