A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3585676



Internal ID18883957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:214018918..214068785hg38UCSC Ensembl
Innerchr2:214883642..214933509hg19UCSC Ensembl
Innerchr2:214591887..214641754hg18UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg3849868
hg1949868
hg1849868
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv999323
Supporting Variants
Samples
Known GenesSPAG16
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3585676
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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