A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039910



Internal ID19129129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:47076675..47703613hg19UCSC Ensembl
Innerchr10:46496681..47173619hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg19626939
hg18676939
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv787n100
Supporting Variantsnssv3512828, nssv3514103, nssv3522423, nssv3503255, nssv3509769
Samples
Known GenesAGAP9, ANTXRL, ANTXRLP1, ANXA8, BMS1P2, BMS1P6, FAM25C, FAM25G, FAM35DP, HNRNPA1P33, LINC00842, LOC100996758, NPY4R
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039910
Frequency
Sample Size11257
Observed Gain4
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer