A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049857



Internal ID19139076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46674168..47910971hg19UCSC Ensembl
Innerchr10:46094174..47430977hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg191236804
hg181336804
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv745n100
Supporting Variantsnssv3517355, nssv3520640
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)nsv1049857
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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