A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17106036



Internal ID21426835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:51345864..51345864hg38UCSC Ensembl
chr19:51849118..51849118hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg38218
hg19218
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5652712
Supporting Variants
SamplesHG00731
Known GenesETFB
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17106036
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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