A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591302



Internal ID16378711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:113824234..113882123hg38UCSC Ensembl
Innerchr3:113543081..113600970hg19UCSC Ensembl
Innerchr3:115025771..115083660hg18UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg3857890
hg1957890
hg1857890
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8506n54
Supporting Variantsnssv1152527
SamplesHGDP00622
Known GenesGRAMD1C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591302
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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