A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17106644



Internal ID21494165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:58337378..58337455hg38UCSC Ensembl
chr19:58848744..58848821hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5593627
Supporting Variants
SamplesNA19238
Known GenesZSCAN22
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17106644
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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