A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051840



Internal ID19141059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:6357004..6369507hg38UCSC Ensembl
Innerchr10:6398966..6411469hg19UCSC Ensembl
Innerchr10:6438972..6451475hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3812504
hg1912504
hg1812504
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3487558, nssv3487713, nssv3707678, nssv3485491, nssv3707676, nssv3483472, nssv3497305, nssv3494302, nssv3493235, nssv3497257, nssv3489708, nssv3707677, nssv3707679, nssv3491287, nssv3486023, nssv3496565, nssv3495427, nssv3488214, nssv3501822, nssv3490550
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051840
Frequency
Sample Size11257
Observed Gain9
Observed Loss11
Observed Complex0
Frequencyn/a


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