A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14311287



Internal ID22204842
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3206644
Supporting Variants
SamplesHG00732
Known GenesSORCS2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14311287
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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