A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002274



Internal ID19091491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:89896137..90208553hg38UCSC Ensembl
Innerchr2:89934947..90247419hg19UCSC Ensembl
Innerchr2:89571989..89884724hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38312417
hg19312473
hg18312736
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3975n100
Supporting Variantsnssv3579815
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)nsv1002274
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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