A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5874166



Internal ID22649117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:4767115..4772287hg38UCSC Ensembl
chr17:4670410..4675582hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg385173
hg195173
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17474504
Samples
Known GenesTM4SF5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5874166
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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