A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3559703



Internal ID22422585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:75763434..75763434hg38UCSC Ensembl
chr11:75474479..75474479hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14357927, nssv14357923, nssv14357924, nssv14357926, nssv14357921, nssv14357922, nssv14357925, nssv14357920
SamplesNA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known GenesLOC283214
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3559703
Frequency
Sample Size9
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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