A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3589514



Internal ID18541109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:25603772..25651960hg38UCSC Ensembl
Innerchr3:25645263..25693451hg19UCSC Ensembl
Innerchr3:25620267..25668455hg18UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg3848189
hg1948189
hg1848189
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1000991
Supporting Variants
Samples
Known GenesTOP2B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3589514
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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