A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012894



Internal ID19102111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:41607307..41655489hg38UCSC Ensembl
Innerchr2:41834447..41882629hg19UCSC Ensembl
Innerchr2:41687951..41736133hg18UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3848183
hg1948183
hg1848183
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3581565
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)nsv1012894
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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