A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17356363



Internal ID22582032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:24715766..24715766hg38UCSC Ensembl
chr12:24868700..24868700hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg38615
hg19615
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5975910
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17356363
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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