A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3695289



Internal ID18646884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:131788536..131906562hg38UCSC Ensembl
Innerchr9:134663923..134781949hg19UCSC Ensembl
Innerchr9:133653744..133771770hg18UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg38118027
hg19118027
hg18118027
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1038424
Supporting Variants
Samples
Known GenesMED27
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3695289
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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