A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5841685



Internal ID22616620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:137528726..137541354hg38UCSC Ensembl
chr5:136864415..136877043hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg3812629
hg1912629
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17495539
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5841685
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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