A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592066



Internal ID16032789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:151796917..151833114hg38UCSC Ensembl
Innerchr3:151514705..151550902hg19UCSC Ensembl
Innerchr3:152997395..153033592hg18UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3836198
hg1936198
hg1836198
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8652n54
Supporting Variantsnssv976841
Samples
Known GenesAADAC, MIR548H2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592066
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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