A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv582368



Internal ID16023091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:85094623..85152929hg38UCSC Ensembl
Innerchr2:85321746..85380052hg19UCSC Ensembl
Innerchr2:85175257..85233563hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg3858307
hg1958307
hg1858307
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv913828
Samples
Known GenesTCF7L1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv582368
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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