A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3580259



Internal ID18531854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:114626816..114646501hg38UCSC Ensembl
Innerchr2:115384393..115404078hg19UCSC Ensembl
Innerchr2:115100863..115120548hg18UCSC Ensembl
Cytoband2q14.1
Allele length
AssemblyAllele length
hg3819686
hg1919686
hg1819686
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1010029
Supporting Variants
Samples
Known GenesDPP10
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3580259
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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