A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3198957



Internal ID22348619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:159734158..159734809hg38UCSC Ensembl
chr3:159451947..159452598hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg38652
hg19652
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14309110, nssv14309109
SamplesHG00731, HG00732
Known GenesIQCJ-SCHIP1, SCHIP1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3198957
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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