A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048919



Internal ID19138138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:47076675..47703282hg19UCSC Ensembl
Innerchr10:46496681..47173288hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg19626608
hg18676608
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv787n100
Supporting Variantsnssv3511103, nssv3514061, nssv3705939
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)nsv1048919
Frequency
Sample Size11257
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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