A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3696409



Internal ID18994690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:133670349..133752683hg38UCSC Ensembl
Innerchr9:136535471..136617805hg19UCSC Ensembl
Innerchr9:135525292..135607626hg18UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3882335
hg1982335
hg1882335
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1049281
Supporting Variants
Samples
Known GenesSARDH
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3696409
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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