A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3197235



Internal ID22347139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:25027412..25033666hg38UCSC Ensembl
chr6:25027640..25033894hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg386255
hg196255
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14326795, nssv14326796
SamplesNA19239, NA19240
Known GenesFAM65B
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3197235
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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