A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050672



Internal ID19139891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46247355..47392320hg19UCSC Ensembl
Innerchr10:45567361..46812326hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg191144966
hg181244966
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv732n100
Supporting Variantsnssv3520074, nssv3508575, nssv3508981, nssv3517579
Samples
Known GenesAGAP4, AGAP9, ANXA8, BMS1P1, BMS1P2, BMS1P5, BMS1P6, FAM21C, FAM25C, FAM25G, FAM35BP, FAM35DP, FRMPD2P1, GLUD1P7, GPRIN2, HNRNPA1P33, LINC00842, LOC100996758, NPY4R, PTPN20A, PTPN20B, SYT15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050672
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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