A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14327904



Internal ID22209266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:75610906..75610993hg38UCSC Ensembl
chr6:76320622..76320709hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV duplication
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3528866
Supporting Variants
SamplesHG00732
Known GenesSENP6
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14327904
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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