A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1000991



Internal ID18743522
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 StatusM
Merged Variantsdgv4707n100
Supporting Variantsnssv3589514
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)nsv1000991
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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