A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17362919



Internal ID22588588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:25085739..25085739hg38UCSC Ensembl
chr12:25238673..25238673hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5978758
Supporting Variants
Samples
Known GenesLRMP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17362919
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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