A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050207



Internal ID18792738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:64496959..65546388hg38UCSC Ensembl
Innerchr10:66256716..67306146hg19UCSC Ensembl
Innerchr10:65926722..66976152hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg381049430
hg191049431
hg181049431
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3707149
Samples
Known GenesANXA2P3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050207
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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