A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3696145



Internal ID18994426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:64493516..64913310hg38UCSC Ensembl
Innerchr9:69505934..69925728hg19UCSC Ensembl
Innerchr9:68795754..69215548hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38419795
hg19419795
hg18419795
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1026163
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)nssv3696145
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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