A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3212637



Internal ID22359818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:137439701..137452800hg38UCSC Ensembl
chr9:140334153..140347252hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3813100
hg1913100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9847n152
Supporting Variantsnssv14349533, nssv14349537, nssv14349539, nssv14349535, nssv14349540, nssv14349536, nssv14349538, nssv14349532, nssv14349534
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known GenesENTPD8, MIR7114, NSMF
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3212637
Frequency
Sample Size9
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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