A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591995



Internal ID16379404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:149245608..149282414hg38UCSC Ensembl
Innerchr3:148963395..149000201hg19UCSC Ensembl
Innerchr3:150446085..150482891hg18UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3836807
hg1936807
hg1836807
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv976493
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591995
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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