A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3583037



Internal ID18534632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:174704308..174757118hg38UCSC Ensembl
Innerchr2:175569036..175621846hg19UCSC Ensembl
Innerchr2:175277282..175330092hg18UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg3852811
hg1952811
hg1852811
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1012645
Supporting Variants
Samples
Known GenesCHRNA1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3583037
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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