A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051450



Internal ID18793981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46286428..46333389hg38UCSC Ensembl
Innerchr10:47657664..47704625hg19UCSC Ensembl
Innerchr10:47127670..47174631hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3846962
hg1946962
hg1846962
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3519364, nssv3504742, nssv3518825
Samples
Known GenesANTXRL
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051450
Frequency
Sample Size29084
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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