A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1000071



Internal ID19089288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:109129646..109176733hg38UCSC Ensembl
Innerchr3:108848493..108895580hg19UCSC Ensembl
Innerchr3:110331183..110378270hg18UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg3847088
hg1947088
hg1847088
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3735250
Samples
Known GenesFLJ22763
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1000071
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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