A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17106310



Internal ID21455046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:56149296..56149369hg38UCSC Ensembl
chr19:56660665..56660738hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5584851
Supporting Variants
SamplesHG02011
Known GenesZNF444
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17106310
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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