A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041665



Internal ID18784196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:71231338..71272698hg38UCSC Ensembl
Innerchr10:72991095..73032455hg19UCSC Ensembl
Innerchr10:72661101..72702461hg18UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3841361
hg1941361
hg1841361
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3513296
Samples
Known GenesUNC5B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041665
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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