A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4432998



Internal ID21395000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:17683074..17683434hg38UCSC Ensembl
chr1:18009569..18009929hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38361
hg19361
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15745766
SamplesSMI034
Known GenesARHGEF10L
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4432998
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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