A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5977149



Internal ID22752084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:80522843..80522843hg38UCSC Ensembl
chr15:80815184..80815184hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17375991
Samples
Known GenesARNT2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5977149
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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