A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17156127



Internal ID21472598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:154368310..154368310hg38UCSC Ensembl
chr6:154689444..154689444hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5639880
Supporting Variants
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17156127
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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