A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5842296



Internal ID22617231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:214046..235767hg38UCSC Ensembl
chr5:214161..235882hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3821722
hg1921722
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17499076
Samples
Known GenesCCDC127, SDHA
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5842296
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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