A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15745766



Internal ID21392201
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 StatusS
Merged Variantsnsv4432998
Supporting Variants
SamplesSMI034
Known GenesARHGEF10L
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15745766
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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