A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17062085



Internal ID21413489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:202205211..202205211hg38UCSC Ensembl
chr1:202174339..202174339hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg382440
hg192440
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5614884
Supporting Variants
SamplesHG00513
Known GenesLGR6
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17062085
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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