A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043563



Internal ID19132782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46674168..47960070hg19UCSC Ensembl
Innerchr10:46094174..47480076hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg191285903
hg181385903
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv745n100
Supporting Variantsnssv3510086
Samples
Known GenesAGAP9, ANTXRL, ANTXRLP1, ANXA8, ANXA8L1, ANXA8L2, BMS1P1, BMS1P2, BMS1P5, BMS1P6, FAM21B, FAM25B, FAM25C, FAM25G, FAM35BP, FAM35DP, FRMPD2P1, GLUD1P7, 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)nsv1043563
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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