A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051110



Internal ID19140329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46169941..46333389hg38UCSC Ensembl
Innerchr10:47541177..47704625hg19UCSC Ensembl
Innerchr10:47011183..47174631hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38163449
hg19163449
hg18163449
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv836n100
Supporting Variantsnssv3521820, nssv3706031, nssv3515072, nssv3706034, nssv3706040, nssv3520783, nssv3518860, nssv3509316, nssv3517004, nssv3515907, nssv3706032, nssv3505256, nssv3517567, nssv3706028, nssv3513870, nssv3706029, nssv3505531, nssv3706033, nssv3508886, nssv3706042, nssv3510993, nssv3504544, nssv3706030, nssv3507477, nssv3706038, nssv3706037, nssv3505549, nssv3706041, nssv3706035, nssv3509224, nssv3508142, nssv3514734, nssv3706043, nssv3706039, nssv3706036
Samples
Known GenesANTXRL, ANTXRLP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051110
Frequency
Sample Size11257
Observed Gain34
Observed Loss1
Observed Complex0
Frequencyn/a


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