A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv776n100



Internal ID22786863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46975048..47108045hg19UCSC Ensembl
chr10:46395054..46528051hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg19132998
hg18132998
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1045396, nsv1040227, nsv1043699, nsv1043880, nsv1037807, nsv1037665, nsv1046066, nsv1035443
Samples
Known GenesGPRIN2, 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)dgv776n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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