A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3693005



Internal ID18991286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:42711968..42856259hg38UCSC Ensembl
Innerchr9:44114860..44259151hg19UCSC Ensembl
Innerchr9:44054856..44199147hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38144292
hg19144292
hg18144292
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1033665
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)nssv3693005
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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