A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17088586



Internal ID21433511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:9221379..9221379hg38UCSC Ensembl
chr12:9373975..9373975hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5655618
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17088586
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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