A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17386377



Internal ID22444247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:32785193..32785193hg38UCSC Ensembl
chr15:33077394..33077394hg19UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38247
hg19247
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5971365
Supporting Variants
Samples
Known GenesFMN1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17386377
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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