A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053674



Internal ID19142893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:47096230..47392320hg19UCSC Ensembl
Innerchr10:46516236..46812326hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg19296091
hg18296091
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv792n100
Supporting Variantsnssv3520502, nssv3509181, nssv3705951, nssv3508392, nssv3516606, nssv3705949, nssv3505180, nssv3522002, nssv3705950, nssv3513123
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)nsv1053674
Frequency
Sample Size11257
Observed Gain9
Observed Loss1
Observed Complex0
Frequencyn/a


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