A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009139



Internal ID19098357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:67878547..67961318hg38UCSC Ensembl
Innerchr2:68105679..68188450hg19UCSC Ensembl
Innerchr2:67959183..68041954hg18UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg3882772
hg1982772
hg1882772
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3577280
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)nsv1009139
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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