A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3697635



Internal ID18995916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:104599429..104609842hg38UCSC Ensembl
Innerchr9:107361710..107372123hg19UCSC Ensembl
Innerchr9:106401531..106411944hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3810414
hg1910414
hg1810414
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1045875
Supporting Variants
Samples
Known GenesOR13C2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3697635
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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