A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015093



Internal ID19104310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:66183355..66203479hg38UCSC Ensembl
Innerchr2:66410487..66430611hg19UCSC Ensembl
Innerchr2:66263991..66284115hg18UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg3820125
hg1920125
hg1820125
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3730858
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)nsv1015093
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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