A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5878910



Internal ID22653876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:28755346..28763013hg38UCSC Ensembl
chr17:27082364..27090031hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg387668
hg197668
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17477530
Samples
Known GenesFAM222B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5878910
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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