A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17143246



Internal ID21482118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:2893191..2893191hg38UCSC Ensembl
chr6:2893425..2893425hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5634208
Supporting Variants
SamplesHG03732
Known GenesSERPINB9
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17143246
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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