A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581670



Internal ID16369079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:44221493..44240905hg38UCSC Ensembl
Innerchr2:44448632..44468044hg19UCSC Ensembl
Innerchr2:44302136..44321548hg18UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3819413
hg1919413
hg1819413
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv907911
Samples
Known GenesPPM1B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581670
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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