A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14338955



Internal ID22149064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:132698175..132698175hg38UCSC Ensembl
chr7:132382934..132382934hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3564722
Supporting Variants
SamplesHG00514
Known GenesFLJ40288
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14338955
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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