A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17148871



Internal ID21474871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:68733737..68733737hg38UCSC Ensembl
chr6:69443629..69443629hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5642590
Supporting Variants
SamplesHG03371
Known GenesBAI3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17148871
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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