A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030357



Internal ID19119576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:69178874..69630327hg19UCSC Ensembl
Innerchr9:68468694..68920147hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg19451454
hg18451454
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7653n100
Supporting Variantsnssv3696077, nssv3759731
Samples
Known GenesANKRD20A4, CBWD5, CBWD6, FOXD4L6, LOC440896
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1030357
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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