A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14329578



Internal ID22260072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:88907354..88907414hg38UCSC Ensembl
chr6:89617073..89617133hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3197313
Supporting Variants
SamplesNA19238
Known GenesRNGTT
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14329578
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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