A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17155580



Internal ID21475469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:132792352..132792352hg38UCSC Ensembl
chr6:133113491..133113491hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5633435
Supporting Variants
SamplesHG03371
Known GenesSLC18B1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17155580
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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