A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4435640



Internal ID21397642
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 StatusM
Merged Variants
Supporting Variantsnssv15754062
SamplesNB08
Known GenesABL1
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4435640
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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