A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044251



Internal ID19133470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:42706775..42751348hg38UCSC Ensembl
Innerchr10:43202223..43246796hg19UCSC Ensembl
Innerchr10:42522229..42566802hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3844574
hg1944574
hg1844574
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv720n100
Supporting Variantsnssv3504428, nssv3508909, nssv3707773, nssv3512103, nssv3513862, nssv3505649, nssv3519841, nssv3707774, nssv3509567, nssv3521826, nssv3518288, nssv3507336, nssv3707775, nssv3522295
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)nsv1044251
Frequency
Sample Size11257
Observed Gain14
Observed Loss0
Observed Complex0
Frequencyn/a


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