A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14331191



Internal ID22194303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:149803494..149803494hg38UCSC Ensembl
chr6:150124630..150124630hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38264
hg19264
Variant TypeCNV alu insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3564320
Supporting Variants
SamplesHG00731
Known GenesPCMT1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
CommentsInsertion of a Alu mobile element relative to the reference
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14331191
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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