A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14335094



Internal ID22195746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:81132103..81132103hg38UCSC Ensembl
chr7:80761419..80761419hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3564842
Supporting Variants
SamplesHG00731
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14335094
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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