A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591345



Internal ID16378754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:116100529..116184054hg38UCSC Ensembl
Innerchr3:115819376..115902901hg19UCSC Ensembl
Innerchr3:117302066..117385591hg18UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg3883526
hg1983526
hg1883526
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv971638
Samples
Known GenesLSAMP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591345
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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