A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3695201



Internal ID18993482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:116836134..116858484hg38UCSC Ensembl
Innerchr9:119598413..119620763hg19UCSC Ensembl
Innerchr9:118638234..118660584hg18UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3822351
hg1922351
hg1822351
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1049877
Supporting Variants
Samples
Known GenesASTN2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3695201
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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