A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008916



Internal ID19098134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:89156915..89192765hg38UCSC Ensembl
Innerchr3:89206065..89241915hg19UCSC Ensembl
Innerchr3:89288755..89324605hg18UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg3835851
hg1935851
hg1835851
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3596284
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)nsv1008916
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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