A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3207925



Internal ID22356250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:497801..509450hg38UCSC Ensembl
chr7:537438..549087hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3811650
hg1911650
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8317n152
Supporting Variantsnssv14332920, nssv14332918, nssv14332922, nssv14332916, nssv14332914, nssv14332921, nssv14332915, nssv14332919, nssv14332917
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known GenesPDGFA
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3207925
Frequency
Sample Size9
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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