A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029511



Internal ID18772042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:33042019..33241605hg38UCSC Ensembl
Innerchr9:33042017..33241603hg19UCSC Ensembl
Innerchr9:33032017..33231603hg18UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38199587
hg19199587
hg18199587
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7515n100
Supporting Variantsnssv3688869
Samples
Known GenesB4GALT1, LOC101929639, SMU1, SPINK4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1029511
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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