A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038081



Internal ID19127300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46169941..46372244hg38UCSC Ensembl
Innerchr10:47541177..47743504hg19UCSC Ensembl
Innerchr10:47011183..47213510hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38202304
hg19202328
hg18202328
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv836n100
Supporting Variantsnssv3706049, nssv3508900, nssv3706044, nssv3706051, nssv3706054, nssv3505413, nssv3522391, nssv3508717, nssv3510667, nssv3521058, nssv3511663, nssv3509627, nssv3706052, nssv3513683, nssv3706056, nssv3706046, nssv3511903, nssv3508054, nssv3504824, nssv3706057, nssv3706050, nssv3521181, nssv3511961, nssv3514978, nssv3706048, nssv3515824, nssv3517382, nssv3505175, nssv3508266, nssv3504572, nssv3520341, nssv3706055, nssv3706047, nssv3706058, nssv3508647, nssv3515401, nssv3516346, nssv3519915, nssv3706045, nssv3507428, nssv3506032, nssv3509278, nssv3706053
Samples
Known GenesANTXRL, ANTXRLP1, FAM25B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038081
Frequency
Sample Size11257
Observed Gain39
Observed Loss4
Observed Complex0
Frequencyn/a


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