A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17367068



Internal ID22592737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:42996332..42996332hg38UCSC Ensembl
chr12:43390135..43390135hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg38200
hg19200
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5968559
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17367068
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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