A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014902



Internal ID19104119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:168407067..168441444hg38UCSC Ensembl
Innerchr2:169263577..169297954hg19UCSC Ensembl
Innerchr2:168971823..169006200hg18UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg3834378
hg1934378
hg1834378
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4102n100
Supporting Variantsnssv3583011, nssv3583012, nssv3583010
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)nsv1014902
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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