A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3695207



Internal ID18993488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:118320206..118365224hg38UCSC Ensembl
Innerchr9:121082484..121127502hg19UCSC Ensembl
Innerchr9:120122305..120167323hg18UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3845019
hg1945019
hg1845019
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1038962
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)nssv3695207
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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