A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18223555



Internal ID20790596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:137598046..137669216hg38UCSC Ensembl
chr9:140492498..140563668hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3871171
hg1971171
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6451331
Supporting Variants
Samples
Known GenesARRDC1, C9orf37, EHMT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18223555
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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