A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14344167



Internal ID22249481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:43697193..43697193hg38UCSC Ensembl
chr10:44192641..44192641hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3559365
Supporting Variants
SamplesHG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14344167
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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