A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5880095



Internal ID22655065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:20286311..20341491hg38UCSC Ensembl
chr17:20189624..20244804hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3855181
hg1955181
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17476166
Samples
Known GenesCCDC144CP, SPECC1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5880095
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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