A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010096



Internal ID19099315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:81280170..81332053hg38UCSC Ensembl
Innerchr2:81507294..81559177hg19UCSC Ensembl
Innerchr2:81360805..81412688hg18UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3851884
hg1951884
hg1851884
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3582117
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)nsv1010096
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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