A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006267



Internal ID19095485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:4153079..4171940hg38UCSC Ensembl
Innerchr2:4200669..4219530hg19UCSC Ensembl
Innerchr2:4178544..4197405hg18UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3818862
hg1918862
hg1818862
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3704n100
Supporting Variantsnssv3726663
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1006267
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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