A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3696138



Internal ID18994419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:64475171..64866653hg38UCSC Ensembl
Innerchr9:69487589..69879071hg19UCSC Ensembl
Innerchr9:68777409..69168891hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38391483
hg19391483
hg18391483
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1018085
Supporting Variants
Samples
Known GenesLOC100133920
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3696138
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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