A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041773



Internal ID19130992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46539691..47122809hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg18583119
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv787n100
Supporting Variantsnssv3512301, nssv3518831
Samples
Known GenesAGAP9, ANTXRLP1, ANXA8, BMS1P2, BMS1P6, FAM25C, FAM25G, FAM35DP, HNRNPA1P33, LINC00842
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041773
Frequency
Sample Size11257
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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