A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041495



Internal ID18784026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46169941..46257664hg38UCSC Ensembl
Innerchr10:47541177..47628900hg19UCSC Ensembl
Innerchr10:47011183..47098906hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3887724
hg1987724
hg1887724
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv831n100
Supporting Variantsnssv3513102
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)nsv1041495
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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