A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14362312



Internal ID22198240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:37102938..37102938hg38UCSC Ensembl
chr1:37568539..37568539hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3561820
Supporting Variants
SamplesHG00732
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14362312
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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