A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050794



Internal ID19140013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:47129684..47742076hg19UCSC Ensembl
Innerchr10:46549690..47212082hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg19612393
hg18662393
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv787n100
Supporting Variantsnssv3513817, nssv3520867
Samples
Known GenesAGAP9, ANTXRL, ANTXRLP1, ANXA8, BMS1P2, BMS1P6, FAM25B, 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)nsv1050794
Frequency
Sample Size11257
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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