A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013851



Internal ID19103070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:235145242..235168266hg38UCSC Ensembl
Innerchr2:236053886..236076910hg19UCSC Ensembl
Innerchr2:235718625..235741649hg18UCSC Ensembl
Cytoband2q37.2
Allele length
AssemblyAllele length
hg3823025
hg1923025
hg1823025
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3586948
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)nsv1013851
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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