A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013631



Internal ID18756163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:77237554..77261362hg38UCSC Ensembl
Innerchr3:77286705..77310513hg19UCSC Ensembl
Innerchr3:77369395..77393203hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg3823809
hg1923809
hg1823809
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3733764
Samples
Known GenesROBO2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1013631
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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