A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17066071



Internal ID21449898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:6868107..6868107hg38UCSC Ensembl
chr1:6928167..6928167hg19UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg38333
hg19333
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5617924
Supporting Variants
SamplesHG01114
Known GenesCAMTA1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17066071
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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