A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17089637



Internal ID21469605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:110201301..110201301hg38UCSC Ensembl
chr13:110853648..110853648hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38231
hg19231
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5645877
Supporting Variants
SamplesHG03125
Known GenesCOL4A1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17089637
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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