A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14336865



Internal ID22198587
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
SamplesHG00732
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Commentscomplex variant
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14336865
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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