A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3564855



Internal ID22433579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:138920170..138920170hg38UCSC Ensembl
chr7:138604916..138604916hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14336976, nssv14336977, nssv14336979, nssv14336980, nssv14336978
SamplesNA19238, NA19239, HG00732, NA19240, HG00733
Known GenesKIAA1549
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3564855
Frequency
Sample Size9
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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