A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17146355



Internal ID21472375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:160152643..160152643hg38UCSC Ensembl
chr6:160573675..160573675hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5626607
Supporting Variants
SamplesHG03125
Known GenesSLC22A1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17146355
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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