A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3580729



Internal ID18532324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:127044799..127104681hg38UCSC Ensembl
Innerchr2:127802375..127862257hg19UCSC Ensembl
Innerchr2:127518845..127578727hg18UCSC Ensembl
Cytoband2q14.3
Allele length
AssemblyAllele length
hg3859883
hg1959883
hg1859883
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1003887
Supporting Variants
Samples
Known GenesBIN1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3580729
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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