A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048921



Internal ID19138140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46674168..47967299hg19UCSC Ensembl
Innerchr10:46094174..47487305hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg191293132
hg181393132
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv745n100
Supporting Variantsnssv3519718
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)nsv1048921
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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