A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589971



Internal ID16377380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:26383758..26397924hg38UCSC Ensembl
Innerchr3:26425249..26439415hg19UCSC Ensembl
Innerchr3:26400253..26414419hg18UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3814167
hg1914167
hg1814167
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8266n54
Supporting Variantsnssv960157, nssv960155, nssv960156
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589971
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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