A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045436



Internal ID19134655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:47108045..47392320hg19UCSC Ensembl
Innerchr10:46528051..46812326hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg19284276
hg18284276
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv792n100
Supporting Variantsnssv3519276, nssv3705957, nssv3521765, nssv3503106, nssv3512028
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)nsv1045436
Frequency
Sample Size11257
Observed Gain2
Observed Loss3
Observed Complex0
Frequencyn/a


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