A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv818n100



Internal ID20152434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46411170..46472778hg38UCSC Ensembl
chr10:47076675..47138582hg19UCSC Ensembl
chr10:46496681..46558588hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3861609
hg1961908
hg1861908
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1035793, nsv1049440, nsv1035331, nsv1048725, nsv1049343, nsv1038846, nsv1046933, nsv1051361
Samples
Known GenesHNRNPA1P33, LINC00842, 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)dgv818n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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