A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17467154



Internal ID22525045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:2739985..2743177hg38UCSC Ensembl
chr12:2849151..2852343hg19UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg383193
hg193193
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5866402
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17467154
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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