A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593633



Internal ID16034356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:8269575..8278313hg38UCSC Ensembl
Innerchr4:8271302..8280040hg19UCSC Ensembl
Innerchr4:8322202..8330940hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg388739
hg198739
hg188739
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8957n54
Supporting Variantsnssv991238
Samples
Known GenesHTRA3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593633
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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