A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14330689



Internal ID22186568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:105909607..105909663hg38UCSC Ensembl
chr6:106357482..106357538hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3527623
Supporting Variants
SamplesHG00731
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14330689
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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