A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14330772



Internal ID22286773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:107149409..107149606hg38UCSC Ensembl
chr6:107470613..107470810hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38198
hg19198
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3528026
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14330772
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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