A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3197166



Internal ID22347074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:38623543..38624256hg38UCSC Ensembl
chr4:38625164..38625877hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38714
hg19714
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14314905
SamplesHG00732
Known GenesFLJ13197
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3197166
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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