A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3586827



Internal ID18885108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:225863170..226017125hg38UCSC Ensembl
Innerchr2:226727886..226881841hg19UCSC Ensembl
Innerchr2:226436130..226590085hg18UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg38153956
hg19153956
hg18153956
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1004080
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)nssv3586827
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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