A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3690673



Internal ID18988954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:18166901..18214880hg38UCSC Ensembl
Innerchr9:18166899..18214878hg19UCSC Ensembl
Innerchr9:18156899..18204878hg18UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3847980
hg1947980
hg1847980
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1034518
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)nssv3690673
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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