A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3696399



Internal ID18647994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:132147299..132243197hg38UCSC Ensembl
Innerchr9:135022686..135118584hg19UCSC Ensembl
Innerchr9:134012507..134108405hg18UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg3895899
hg1995899
hg1895899
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1035219
Supporting Variants
Samples
Known GenesNTNG2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3696399
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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