A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008702



Internal ID18751233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:79536661..79582580hg38UCSC Ensembl
Innerchr2:79763787..79809706hg19UCSC Ensembl
Innerchr2:79617295..79663214hg18UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3845920
hg1945920
hg1845920
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3732007
Samples
Known GenesCTNNA2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1008702
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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