A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17453506



Internal ID22511380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:3933415..3935614hg38UCSC Ensembl
chr12:4042581..4044780hg19UCSC Ensembl
Cytoband12p13.32
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5859366
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17453506
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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