A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5836963



Internal ID22611898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:108997400..109040932hg38UCSC Ensembl
chr4:109918556..109962088hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3843533
hg1943533
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17492239
Samples
Known GenesCOL25A1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5836963
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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