A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001307



Internal ID19090524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:35765257..35900266hg38UCSC Ensembl
Innerchr3:35806749..35941758hg19UCSC Ensembl
Innerchr3:35781753..35916762hg18UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38135010
hg19135010
hg18135010
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4717n100
Supporting Variantsnssv3739692, nssv3739693, nssv3589648, nssv3589647, nssv3589646, nssv3589645, nssv3589649
Samples
Known GenesARPP21
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1001307
Frequency
Sample Size11257
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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