A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5878254



Internal ID22653219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:9252275..9269032hg38UCSC Ensembl
chr17:9155592..9172349hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3816758
hg1916758
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17477080
Samples
Known GenesSTX8
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5878254
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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