A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3695155



Internal ID18646750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:114191459..114680719hg38UCSC Ensembl
Innerchr9:116953739..117442999hg19UCSC Ensembl
Innerchr9:115993560..116482820hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38489261
hg19489261
hg18489261
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1050991
Supporting Variants
Samples
Known GenesAKNA, ATP6V1G1, C9orf91, COL27A1, DFNB31, LOC100505478, MIR455, ORM1, ORM2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3695155
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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