A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008842



Internal ID19098060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:102911841..102943219hg38UCSC Ensembl
Innerchr2:103528299..103559677hg19UCSC Ensembl
Innerchr2:102894731..102926109hg18UCSC Ensembl
Cytoband2q12.1
Allele length
AssemblyAllele length
hg3831379
hg1931379
hg1831379
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3580100
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)nsv1008842
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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