A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009734



Internal ID18752265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:42380771..42429779hg38UCSC Ensembl
Innerchr2:42607911..42656919hg19UCSC Ensembl
Innerchr2:42461415..42510423hg18UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3849009
hg1949009
hg1849009
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3581572
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)nsv1009734
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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