A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17132723



Internal ID21407838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:37901687..37901687hg38UCSC Ensembl
chr4:37903308..37903308hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38133
hg19133
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5611422
Supporting Variants
SamplesHG00512
Known GenesTBC1D1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17132723
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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