A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3208638



Internal ID22356842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:39660415..39666954hg38UCSC Ensembl
chr4:39662035..39668574hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg386540
hg196540
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14314952, nssv14314948, nssv14314949, nssv14314950, nssv14314951, nssv14314946, nssv14314953, nssv14314947, nssv14314954
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3208638
Frequency
Sample Size9
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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