A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052433



Internal ID18794964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46169941..46286428hg38UCSC Ensembl
Innerchr10:47541177..47657664hg19UCSC Ensembl
Innerchr10:47011183..47127670hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38116488
hg19116488
hg18116488
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv832n100
Supporting Variantsnssv3520673, nssv3503309, nssv3514876, nssv3516831, nssv3517356
Samples
Known GenesANTXRLP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052433
Frequency
Sample Size29084
Observed Gain3
Observed Loss2
Observed Complex0
Frequencyn/a


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