A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3695206



Internal ID18993487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:117800990..117926645hg38UCSC Ensembl
Innerchr9:120563268..120688923hg19UCSC Ensembl
Innerchr9:119603089..119728744hg18UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg38125656
hg19125656
hg18125656
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1047685
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3695206
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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