A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3586821



Internal ID18885102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:220354164..220397397hg38UCSC Ensembl
Innerchr2:221218885..221262118hg19UCSC Ensembl
Innerchr2:220927129..220970362hg18UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg3843234
hg1943234
hg1843234
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv997845
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)nssv3586821
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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