A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17103231



Internal ID21443010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:1627913..1627913hg38UCSC Ensembl
chr19:1627912..1627912hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38546
hg19546
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5653180
Supporting Variants
SamplesHG00732
Known GenesTCF3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17103231
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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