A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17366913



Internal ID22592582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:64524637..64526631hg38UCSC Ensembl
chr12:64918417..64920411hg19UCSC Ensembl
Cytoband12q14.2
Allele length
AssemblyAllele length
hg381995
hg191995
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5943251
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17366913
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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