A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591975



Internal ID16379384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:149232993..149249548hg38UCSC Ensembl
Innerchr3:148950780..148967335hg19UCSC Ensembl
Innerchr3:150433470..150450025hg18UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3816556
hg1916556
hg1816556
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8637n54
Supporting Variantsnssv976386, nssv976387
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591975
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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