A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17090948



Internal ID21469809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:53184098..53184159hg38UCSC Ensembl
chr12:53577882..53577943hg19UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5596607
Supporting Variants
SamplesHG03125
Known GenesZNF740
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17090948
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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