A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009069



Internal ID19098287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:164069340..164605431hg38UCSC Ensembl
Innerchr3:163787128..164323219hg19UCSC Ensembl
Innerchr3:165269822..165805913hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38536092
hg19536092
hg18536092
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3614535
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1009069
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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