A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593762



Internal ID16381171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:15002329..15004357hg38UCSC Ensembl
Innerchr4:15003953..15005981hg19UCSC Ensembl
Innerchr4:14613051..14615079hg18UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg382029
hg192029
hg182029
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8977n54
Supporting Variantsnssv993088
Samples
Known GenesCPEB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593762
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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