A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17449979



Internal ID22507850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:88592705..88595342hg38UCSC Ensembl
chr12:88986482..88989119hg19UCSC Ensembl
Cytoband12q21.32
Allele length
AssemblyAllele length
hg382638
hg192638
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5860003
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17449979
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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