A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17092149



Internal ID21453683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:30839194..30839278hg38UCSC Ensembl
chr13:31413331..31413415hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5595540
Supporting Variants
SamplesHG02011
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17092149
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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