A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045663



Internal ID19134882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:15669295..15740136hg38UCSC Ensembl
Innerchr12:15822229..15893070hg19UCSC Ensembl
Innerchr12:15713496..15784337hg18UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg3870842
hg1970842
hg1870842
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3515430
Samples
Known GenesEPS8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045663
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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