A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17106309



Internal ID21441353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:56149026..56149134hg38UCSC Ensembl
chr19:56660395..56660503hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5596027
Supporting Variants
SamplesHG00732
Known GenesZNF444
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17106309
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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