A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5827917



Internal ID22602852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:111196341..111215626hg38UCSC Ensembl
chr1:111738963..111758248hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3819286
hg1919286
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17457116
Samples
Known GenesDENND2D
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5827917
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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