A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3586833



Internal ID18538428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:226507455..226692923hg38UCSC Ensembl
Innerchr2:227372171..227557639hg19UCSC Ensembl
Innerchr2:227080415..227265883hg18UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg38185469
hg19185469
hg18185469
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1011562
Supporting Variants
Samples
Known GenesMIR5702
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3586833
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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