A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590622



Internal ID16378031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:72730992..72735474hg38UCSC Ensembl
Innerchr3:72780143..72784625hg19UCSC Ensembl
Innerchr3:72862833..72867315hg18UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg384483
hg194483
hg184483
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8377n54
Supporting Variantsnssv965569, nssv965570
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590622
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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