A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv773n100



Internal ID22786860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46961233..47743504hg19UCSC Ensembl
chr10:46381239..47213510hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg19782272
hg18832272
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1049711, nsv1053981, nsv1037588, nsv1047795, nsv1035678, nsv1052564, nsv1053988, nsv1050068
Samples
Known GenesAGAP9, ANTXRL, ANTXRLP1, ANXA8, BMS1P2, BMS1P6, FAM25B, FAM25C, FAM25G, FAM35DP, GPRIN2, HNRNPA1P33, LINC00842, LOC100996758, NPY4R, SYT15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv773n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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