A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011029



Internal ID19100246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:240154545..240182136hg38UCSC Ensembl
Innerchr2:241093962..241121553hg19UCSC Ensembl
Innerchr2:240742635..240770226hg18UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg3827592
hg1927592
hg1827592
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3586980
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)nsv1011029
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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