A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5855081



Internal ID22630016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:51451423..51453140hg38UCSC Ensembl
chr13:52025559..52027276hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg381718
hg191718
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17466194, nssv17458906
Samples
Known GenesINTS6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5855081
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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