A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17138369



Internal ID21509802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:26652243..26652243hg38UCSC Ensembl
chr4:26653865..26653865hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38348
hg19348
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5610960
Supporting Variants
SamplesNA20847
Known GenesTBC1D19
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17138369
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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