A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3527832



Internal ID22397219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:98140130..98140197hg38UCSC Ensembl
chr7:97769442..97769509hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8661n152
Supporting Variantsnssv14335549, nssv14335551, nssv14335554, nssv14335552, nssv14335550, nssv14335553
SamplesNA19238, NA19239, HG00731, HG00732, NA19240, HG00733
Known GenesLMTK2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3527832
Frequency
Sample Size9
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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