A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039304



Internal ID18781835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:1157778..1245720hg38UCSC Ensembl
Innerchr10:1203718..1287772hg19UCSC Ensembl
Innerchr10:1193718..1277772hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3887943
hg1984055
hg1884055
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv656n100
Supporting Variantsnssv3486149
Samples
Known GenesADARB2, LINC00200
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039304
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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