A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17106551



Internal ID21494142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:7944971..7945438hg38UCSC Ensembl
chr19:8009856..8010323hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38468
hg19468
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5603555
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17106551
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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