A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17141719



Internal ID21508725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:43313039..43313039hg38UCSC Ensembl
chr6:43280777..43280777hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38888
hg19888
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5631195
Supporting Variants
SamplesNA20847
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17141719
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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