A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593476



Internal ID16034199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:4341513..4353653hg38UCSC Ensembl
Innerchr4:4343240..4355380hg19UCSC Ensembl
Innerchr4:4394141..4406281hg18UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg3812141
hg1912141
hg1812141
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152586
SamplesNINDS_20
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593476
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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