A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18233777



Internal ID20800817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:104772132..104772729hg38UCSC Ensembl
chr9:107534413..107535010hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38598
hg19598
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6452218
Supporting Variants
Samples
Known GenesNIPSNAP3B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18233777
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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