A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008672



Internal ID19097889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:51044124..51110446hg38UCSC Ensembl
Innerchr2:51271262..51337584hg19UCSC Ensembl
Innerchr2:51124766..51191088hg18UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg3866323
hg1966323
hg1866323
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3814n100
Supporting Variantsnssv3581687
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)nsv1008672
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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