A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3689238



Internal ID18640833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:11575785..11799681hg38UCSC Ensembl
Innerchr9:11575785..11799681hg19UCSC Ensembl
Innerchr9:11565785..11789681hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38223897
hg19223897
hg18223897
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1017027
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)nssv3689238
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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