A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv755n100



Internal ID22786842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46918172..47392320hg19UCSC Ensembl
chr10:46338178..46812326hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg19474149
hg18474149
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1037469, nsv1041566, nsv1036465, nsv1035208, nsv1035557, nsv1043950, nsv1054698, nsv1039110
Samples
Known GenesAGAP9, ANXA8, BMS1P2, BMS1P6, FAM25C, FAM25G, FAM35BP, 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)dgv755n100
Frequency
Sample Size11257
Observed Gain57
Observed Loss25
Observed Complex0
Frequencyn/a


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