A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049989



Internal ID18792520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46305526..46332377hg38UCSC Ensembl
Innerchr10:47676762..47703613hg19UCSC Ensembl
Innerchr10:47146768..47173619hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3826852
hg1926852
hg1826852
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv847n100
Supporting Variantsnssv3519272
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)nsv1049989
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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