A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019829



Internal ID18762364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:33042019..33237213hg38UCSC Ensembl
Innerchr9:33042017..33237211hg19UCSC Ensembl
Innerchr9:33032017..33227211hg18UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38195195
hg19195195
hg18195195
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7515n100
Supporting Variantsnssv3688868
Samples
Known GenesB4GALT1, LOC101929639, SMU1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019829
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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