A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015137



Internal ID19104354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:43298688..43339575hg38UCSC Ensembl
Innerchr2:43525827..43566714hg19UCSC Ensembl
Innerchr2:43379331..43420218hg18UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3840888
hg1940888
hg1840888
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3581578
Samples
Known GenesTHADA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015137
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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