A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5840287



Internal ID22615222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:10246259..10247958hg38UCSC Ensembl
chr5:10246371..10248070hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17492296, nssv17499302
Samples
Known GenesFAM173B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5840287
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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