A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005711



Internal ID19094928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:153568415..153680824hg38UCSC Ensembl
Innerchr3:153286204..153398613hg19UCSC Ensembl
Innerchr3:154768894..154881303hg18UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg38112410
hg19112410
hg18112410
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3606342
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)nsv1005711
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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