A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003879



Internal ID19093097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:45104765..45124728hg38UCSC Ensembl
Innerchr2:45331904..45351867hg19UCSC Ensembl
Innerchr2:45185408..45205371hg18UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3819964
hg1919964
hg1819964
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3803n100
Supporting Variantsnssv3581608
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)nsv1003879
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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