A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593615



Internal ID16381024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:7524012..7542883hg38UCSC Ensembl
Innerchr4:7525739..7544610hg19UCSC Ensembl
Innerchr4:7576639..7595510hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3818872
hg1918872
hg1818872
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8954n54
Supporting Variantsnssv1152622
SamplesHGDP01027
Known GenesSORCS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593615
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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