A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5881335



Internal ID22656310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:75171109..75172608hg38UCSC Ensembl
chr17:73167204..73168703hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17478927, nssv17475922
Samples
Known GenesSUMO2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5881335
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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