A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041131



Internal ID19130350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46169941..46332377hg38UCSC Ensembl
Innerchr10:47541177..47703613hg19UCSC Ensembl
Innerchr10:47011183..47173619hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38162437
hg19162437
hg18162437
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv836n100
Supporting Variantsnssv3520247, nssv3507139, nssv3518752, nssv3513363, nssv3510903, nssv3706027, nssv3517804, nssv3520674, nssv3706026, nssv3507787, nssv3706025, nssv3518938
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)nsv1041131
Frequency
Sample Size11257
Observed Gain10
Observed Loss2
Observed Complex0
Frequencyn/a


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