A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589788



Internal ID16377197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:15802839..15804825hg38UCSC Ensembl
Innerchr3:15844346..15846332hg19UCSC Ensembl
Innerchr3:15819350..15821336hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg381987
hg191987
hg181987
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8237n54
Supporting Variantsnssv959459, nssv959461, nssv959460
Samples
Known GenesANKRD28
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589788
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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