A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4432986



Internal ID21394988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:168119806..168122236hg38UCSC Ensembl
chr1:168089044..168091474hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg382431
hg192431
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15749537, nssv15752478
SamplesNB12, NB11
Known GenesGPR161
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4432986
Frequency
Sample Size15
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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