A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589719



Internal ID16377128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:12921716..12960431hg38UCSC Ensembl
Innerchr3:12963216..13001931hg19UCSC Ensembl
Innerchr3:12938216..12976931hg18UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3838716
hg1938716
hg1838716
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv959131
Samples
Known GenesIQSEC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589719
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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