A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5857171



Internal ID22632106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:87515645..87517493hg38UCSC Ensembl
chr13:88167900..88169748hg19UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg381849
hg191849
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17457057, nssv17465143
Samples
Known GenesMIR4500HG
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5857171
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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