A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17103170



Internal ID21448962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:14250688..14251620hg38UCSC Ensembl
chr19:14361500..14362432hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg38933
hg19933
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5601032
Supporting Variants
SamplesHG00864
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17103170
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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