A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045141



Internal ID18787672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:5384177..5449996hg38UCSC Ensembl
Innerchr10:5426140..5491959hg19UCSC Ensembl
Innerchr10:5416140..5481959hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3865820
hg1965820
hg1865820
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3487540
Samples
Known GenesNET1, TUBAL3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045141
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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