A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15754062



Internal ID21389027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:130844167..130847799hg38UCSC Ensembl
chr9:133719554..133723186hg19UCSC Ensembl
Cytoband9q34.12
Allele length
AssemblyAllele length
hg383633
hg193633
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4435640
Supporting Variants
SamplesNB08
Known GenesABL1
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15754062
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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