A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039110



Internal ID19128329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46963600..47392320hg19UCSC Ensembl
Innerchr10:46383606..46812326hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg19428721
hg18428721
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv755n100
Supporting Variantsnssv3709064, nssv3521681
Samples
Known GenesAGAP9, ANXA8, BMS1P2, BMS1P6, FAM25C, FAM25G, FAM35DP, 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)nsv1039110
Frequency
Sample Size11257
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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