A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043526



Internal ID18786057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46169941..46269856hg38UCSC Ensembl
Innerchr10:47541177..47641092hg19UCSC Ensembl
Innerchr10:47011183..47111098hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3899916
hg1999916
hg1899916
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv830n100
Supporting Variantsnssv3507808, nssv3510939, nssv3503509
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)nsv1043526
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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