A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591501



Internal ID16378910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:126301523..126330591hg38UCSC Ensembl
Innerchr3:126020366..126049434hg19UCSC Ensembl
Innerchr3:127503056..127532124hg18UCSC Ensembl
Cytoband3q21.2
Allele length
AssemblyAllele length
hg3829069
hg1929069
hg1829069
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8547n54
Supporting Variantsnssv972407
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591501
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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