A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007758



Internal ID19096977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:35754819..35900266hg38UCSC Ensembl
Innerchr3:35796311..35941758hg19UCSC Ensembl
Innerchr3:35771315..35916762hg18UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38145448
hg19145448
hg18145448
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4717n100
Supporting Variantsnssv3589602, nssv3589601, nssv3589603, nssv3739673
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)nsv1007758
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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