A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005603



Internal ID18748134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:89125002..89174309hg38UCSC Ensembl
Innerchr3:89174152..89223459hg19UCSC Ensembl
Innerchr3:89256842..89306149hg18UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg3849308
hg1949308
hg1849308
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3596283
Samples
Known GenesEPHA3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1005603
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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