A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591841



Internal ID16379250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:136302814..136307010hg38UCSC Ensembl
Innerchr3:136021656..136025852hg19UCSC Ensembl
Innerchr3:137504346..137508542hg18UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg384197
hg194197
hg184197
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8613n54
Supporting Variantsnssv974755, nssv974756
Samples
Known GenesPCCB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591841
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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