A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590996



Internal ID16378405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:95138313..95195446hg38UCSC Ensembl
Innerchr3:94857157..94914290hg19UCSC Ensembl
Innerchr3:96339847..96396980hg18UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3857134
hg1957134
hg1857134
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8445n54
Supporting Variantsnssv967790
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590996
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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