A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4435642



Internal ID21397644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:131101638..131106914hg38UCSC Ensembl
chr9:133977025..133982301hg19UCSC Ensembl
Cytoband9q34.12
Allele length
AssemblyAllele length
hg385277
hg195277
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15753990
SamplesNB08
Known GenesAIF1L
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4435642
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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