A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5880181



Internal ID22655151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:5021725..5022795hg38UCSC Ensembl
chr17:4925020..4926090hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg381071
hg191071
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17478823
Samples
Known GenesKIF1C
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5880181
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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