A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591349



Internal ID16378758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:118476754..118510523hg38UCSC Ensembl
Innerchr3:118195601..118229370hg19UCSC Ensembl
Innerchr3:119678291..119712060hg18UCSC Ensembl
Cytoband3q13.32
Allele length
AssemblyAllele length
hg3833770
hg1933770
hg1833770
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152532
Samples1780862433_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591349
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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