A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036902



Internal ID19126121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:47090539..47392320hg19UCSC Ensembl
Innerchr10:46510545..46812326hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg19301782
hg18301782
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv792n100
Supporting Variantsnssv3705946, nssv3521249, nssv3512999, nssv3507722, nssv3515438, nssv3512615
Samples
Known GenesAGAP9, 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)nsv1036902
Frequency
Sample Size11257
Observed Gain4
Observed Loss2
Observed Complex0
Frequencyn/a


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