A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043611



Internal ID18786142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:116372164..116538288hg38UCSC Ensembl
Innerchr9:119134443..119300567hg19UCSC Ensembl
Innerchr9:118174264..118340388hg18UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg38166125
hg19166125
hg18166125
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7707n100
Supporting Variantsnssv3695166
Samples
Known GenesASTN2, LOC100128505, PAPPA, PAPPA-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1043611
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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