A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17103136



Internal ID21443054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:12292301..12294047hg38UCSC Ensembl
chr19:12403116..12404862hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381747
hg191747
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5592100
Supporting Variants
SamplesHG00732
Known GenesZNF44
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17103136
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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