A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3697651



Internal ID18649246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:108687608..108841186hg38UCSC Ensembl
Innerchr9:111449888..111603466hg19UCSC Ensembl
Innerchr9:110489709..110643287hg18UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38153579
hg19153579
hg18153579
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1046658
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)nssv3697651
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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