A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17453590



Internal ID22511464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:27980598..27989997hg38UCSC Ensembl
chr12:28133531..28142930hg19UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg389400
hg199400
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5848951
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17453590
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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