A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3206644



Internal ID22355156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:7732801..7746100hg38UCSC Ensembl
chr4:7734528..7747827hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3813300
hg1913300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14311283, nssv14311286, nssv14311287, nssv14311289, nssv14311288, nssv14311284, nssv14311290, nssv14311285, nssv14311291
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known GenesSORCS2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3206644
Frequency
Sample Size9
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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