A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008293



Internal ID19097512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:89337939..89368137hg38UCSC Ensembl
Innerchr3:89387089..89417287hg19UCSC Ensembl
Innerchr3:89469779..89499977hg18UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg3830199
hg1930199
hg1830199
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4805n100
Supporting Variantsnssv3596294
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)nsv1008293
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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