A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012916



Internal ID19102133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:44112473..44138696hg38UCSC Ensembl
Innerchr2:44339612..44365835hg19UCSC Ensembl
Innerchr2:44193116..44219339hg18UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3826224
hg1926224
hg1826224
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3581587
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)nsv1012916
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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