A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14328609



Internal ID22266880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:77715888..77726904hg38UCSC Ensembl
chr6:78425605..78436621hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3811017
hg1911017
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3194559
Supporting Variants
SamplesNA19238
Known GenesMEI4
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14328609
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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