A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012445



Internal ID19101662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:35763779..35892079hg38UCSC Ensembl
Innerchr3:35805271..35933571hg19UCSC Ensembl
Innerchr3:35780275..35908575hg18UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38128301
hg19128301
hg18128301
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4717n100
Supporting Variantsnssv3589640, nssv3589639
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)nsv1012445
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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