A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3692424



Internal ID18990705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:5828435..5850834hg38UCSC Ensembl
Innerchr9:5828435..5850834hg19UCSC Ensembl
Innerchr9:5818435..5840834hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3822400
hg1922400
hg1822400
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1016365
Supporting Variants
Samples
Known GenesERMP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3692424
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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