A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17105578



Internal ID21472191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:44273995..44274078hg38UCSC Ensembl
chr19:44778148..44778231hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5602008
Supporting Variants
SamplesHG03125
Known GenesZNF233
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17105578
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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