A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592077



Internal ID16379486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:154617173..154736740hg38UCSC Ensembl
Innerchr3:154334962..154454529hg19UCSC Ensembl
Innerchr3:155817656..155937223hg18UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg38119568
hg19119568
hg18119568
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8656n54
Supporting Variantsnssv1151814
SamplesHGDP00941
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592077
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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