A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv814n100



Internal ID20152430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46428386..46487142hg38UCSC Ensembl
chr10:47062299..47121369hg19UCSC Ensembl
chr10:46482305..46541375hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3858757
hg1959071
hg1859071
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1042344, nsv1039093, nsv1036859, nsv1052787, nsv1052322, nsv1036211, nsv1051022, nsv1045044
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)dgv814n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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