A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036598



Internal ID18779129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46568009..46631445hg38UCSC Ensembl
Innerchr10:46918172..46981608hg19UCSC Ensembl
Innerchr10:46338178..46401614hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3863437
hg1963437
hg1863437
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv747n100
Supporting Variantsnssv3507247, nssv3518097, nssv3514727, nssv3507079, nssv3509099, nssv3508536, nssv3518669, nssv3506675, nssv3521673, nssv3505842, nssv3521856, nssv3507571, nssv3522730, nssv3516291, nssv3517313, nssv3519197, nssv3512569, nssv3510930, nssv3510026, nssv3509464, nssv3517779, nssv3518755, nssv3512112
Samples
Known GenesFAM35BP, SYT15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036598
Frequency
Sample Size29084
Observed Gain10
Observed Loss13
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer