A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052519



Internal ID19141738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:5623495..5675162hg38UCSC Ensembl
Innerchr10:5665458..5717125hg19UCSC Ensembl
Innerchr10:5705464..5757131hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3851668
hg1951668
hg1851668
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv665n100
Supporting Variantsnssv3500861, nssv3486842, nssv3501693, nssv3497973, nssv3498156, nssv3489630, nssv3487662, nssv3483029, nssv3501647, nssv3496329, nssv3492919, nssv3489890, nssv3488749, nssv3482864, nssv3490868, nssv3502066, nssv3491766, nssv3496267, nssv3488572, nssv3499962, nssv3502438, nssv3498273, nssv3496550, nssv3500371
Samples
Known GenesASB13
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052519
Frequency
Sample Size11257
Observed Gain24
Observed Loss0
Observed Complex0
Frequencyn/a


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