A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039093



Internal ID18781624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46432210..46481242hg38UCSC Ensembl
Innerchr10:47068215..47117543hg19UCSC Ensembl
Innerchr10:46488221..46537549hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3849033
hg1949329
hg1849329
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv814n100
Supporting Variantsnssv3507047
Samples
Known GenesLINC00842, LOC100996758, NPY4R
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039093
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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