A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3688869



Internal ID18640464
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 StatusS
Merged Variantsnsv1029511
Supporting Variants
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)nssv3688869
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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