A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14336867



Internal ID22253812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:105908614..105908722hg38UCSC Ensembl
chr7:105549060..105549168hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeOTHER complex substitution
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3522870
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Commentscomplex variant
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14336867
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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