A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039518



Internal ID18782049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46260729..46281263hg38UCSC Ensembl
Innerchr10:47631965..47652499hg19UCSC Ensembl
Innerchr10:47101971..47122505hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3820535
hg1920535
hg1820535
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3506007
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)nsv1039518
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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