A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5867699



Internal ID22642634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:40825729..40833034hg38UCSC Ensembl
chr17:38981981..38989286hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg387306
hg197306
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17473753
Samples
Known GenesTMEM99
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5867699
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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