A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036582



Internal ID19125801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:47136996..47743504hg19UCSC Ensembl
Innerchr10:46557002..47213510hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg19606509
hg18656509
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv787n100
Supporting Variantsnssv3514906, nssv3522526, nssv3503707
Samples
Known GenesAGAP9, ANTXRL, ANTXRLP1, ANXA8, BMS1P2, BMS1P6, FAM25B, FAM25C, FAM25G, FAM35DP, LINC00842
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036582
Frequency
Sample Size11257
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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