A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2801075



Internal ID21246415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:17683146..17683313hg38UCSC Ensembl
chr1:18009641..18009808hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38168
hg19168
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13695039
Samples
Known GenesARHGEF10L
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2801075
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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