A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005142



Internal ID19094359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:162567179..162730030hg38UCSC Ensembl
Innerchr3:162284967..162447818hg19UCSC Ensembl
Innerchr3:163767661..163930512hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38162852
hg19162852
hg18162852
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3607969
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)nsv1005142
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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