A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045959



Internal ID18788490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46169941..46329229hg38UCSC Ensembl
Innerchr10:47541177..47700465hg19UCSC Ensembl
Innerchr10:47011183..47170471hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38159289
hg19159289
hg18159289
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv835n100
Supporting Variantsnssv3522503, nssv3515328, nssv3514793, nssv3506669, nssv3509254, nssv3706022, nssv3706021, nssv3706023, nssv3511651, nssv3509785, nssv3507203, nssv3509700, nssv3504838, nssv3517395
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)nsv1045959
Frequency
Sample Size29084
Observed Gain14
Observed Loss0
Observed Complex0
Frequencyn/a


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