A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17159559



Internal ID21472037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:31454804..31454804hg38UCSC Ensembl
chr6:31422581..31422581hg19UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5627390
Supporting Variants
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17159559
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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