A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv594107



Internal ID16381516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:45336223..45434377hg38UCSC Ensembl
Innerchr4:45338240..45436394hg19UCSC Ensembl
Innerchr4:45032997..45131151hg18UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg3898155
hg1998155
hg1898155
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv996904
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv594107
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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