A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5872038



Internal ID22646976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:14189144..14190708hg38UCSC Ensembl
chr17:14092461..14094025hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg381565
hg191565
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17480367
Samples
Known GenesCOX10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5872038
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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