A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5871802



Internal ID22646740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:19814873..19816124hg38UCSC Ensembl
chr17:19718186..19719437hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg381252
hg191252
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17476156
Samples
Known GenesULK2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5871802
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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