A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18227295



Internal ID20794335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:88386101..88389600hg38UCSC Ensembl
chr9:91001016..91004515hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg383500
hg193500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6445139
Supporting Variants
Samples
Known GenesSPIN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18227295
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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